AMSCO ENDOSCOPY TABLE— 510(k) K821749

Name: FDA 510(k) clearance K821749
Creator: U.S. Food and Drug Administration
Published: 1982-07-09

Substantially Equivalent

American Sterilizer Co.

FDA 510(k) clearance K821749 for AMSCO ENDOSCOPY TABLE, Substantially Equivalent on 1982-07-09. Applicant: American Sterilizer Co.. Device class: 1.

Clearance details

Applicant: American Sterilizer Co.
Product code: Code GDC
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1982-06-15
Decision date: 1982-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GDC

product code GDC

Malfunction: 791
Total: 791

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.