DRENOVAC— 510(k) K883982

Name: FDA 510(k) clearance K883982
Creator: U.S. Food and Drug Administration
Published: 1989-02-23

Substantially Equivalent

Iberhospitex, S.A.

FDA 510(k) clearance K883982 for DRENOVAC, Substantially Equivalent on 1989-02-23. Applicant: Iberhospitex, S.A.. Device class: 1.

Clearance details

Applicant: Iberhospitex, S.A.
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1988-09-20
Decision date: 1989-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Barcelona, Spain, ES

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.