NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC— 510(k) K863201

Name: FDA 510(k) clearance K863201
Creator: U.S. Food and Drug Administration
Published: 1986-08-29

Substantially Equivalent

Allergan, Inc.

FDA 510(k) clearance K863201 for NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC, Substantially Equivalent on 1986-08-29. Applicant: Allergan, Inc.. Device class: 1.

Clearance details

Applicant: Allergan, Inc.
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1986-08-19
Decision date: 1986-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GCY

product code GCY

Malfunction: 786
Other: 1
Total: 787

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.