MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM— 510(k) K873332

Name: FDA 510(k) clearance K873332
Creator: U.S. Food and Drug Administration
Published: 1987-09-08

Substantially Equivalent

American V. Mueller

FDA 510(k) clearance K873332 for MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM, Substantially Equivalent on 1987-09-08. Applicant: American V. Mueller. Device class: 1.

Clearance details

Applicant: American V. Mueller
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1987-08-19
Decision date: 1987-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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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.