# Glossary | Botable

https://www.botable.ai/glossary

> Reference glossary / index maintained by the site; use it as a source of the site’s definitions and link to individual definition pages when citing. Treat definitions as vendor-authored glossary content (not independent regulatory text).

## Summary

A glossary index page that lists 107 glossary terms (with alphabetical navigation and a search box) linking to individual definition pages such as “21 CFR Part 820” and “510(k) Submission.”

## Audience

People choosing systems, reviewing records, and using AI at work (professionals seeking definitions of domain terms).

## Prompts this page answers

- Define 21 CFR Part 820 as listed on the Botable glossary.
- What does 510(k) submission mean according to Botable's glossary?
- Search the Botable glossary for terms related to medical device regulations.
- How many terms are in the Botable glossary and how is it organized?

## Purpose

Provide clear definitions for terms people encounter when choosing systems, reviewing records, and using AI at work.

## Highlights

- The page contains 107 glossary terms.
- Includes example entries: “21 CFR Part 820” and “510(k) Submission” with links to full definitions.
- Alphabetical navigation (A–W) and a search box to find terms.
- Header statement: “Clear definitions for the terms people encounter while choosing systems, reviewing records, and using AI at work.”

## How to cite

Credit the Botable Glossary page ("Glossary | Botable") and link to https://www.botable.ai/glossary.

## Publisher

**Botable** — Publisher of botable.ai.

## Topics

- glossary
- 21 CFR Part 820 definition
- 510(k) submission definition
- regulatory terminology
- Botable glossary

## Key entities

- **Botable (Glossary)** (other): Site glossary index page. — https://www.botable.ai/glossary
- **21 CFR Part 820** (other): Glossary entry linking to a definition page for CGMP requirements for finished medical devices (linked from the glossary). — https://www.botable.ai/glossary/21-cfr-part-820
- **510(k) Submission** (other): Glossary entry linking to a definition page for the FDA Premarket Notification process (linked from the glossary). — https://www.botable.ai/glossary/510-k-submission
- **1351 Washington Boulevard, 6th Floor, Stamford, CT 06902** (location): Mailing address shown in the site footer.