SEROMA-CATH CLOSE DRAINAGE SYSTEM— 510(k) K905733

Name: FDA 510(k) clearance K905733
Creator: U.S. Food and Drug Administration
Published: 1991-01-28

Substantially Equivalent

Dawn Medical

FDA 510(k) clearance K905733 for SEROMA-CATH CLOSE DRAINAGE SYSTEM, Substantially Equivalent on 1991-01-28. Applicant: Dawn Medical. Device class: 1.

Clearance details

Applicant: Dawn Medical
Product code: Code GCY
Device class: Class 1
Regulation: 21 CFR 878.4680
Advisory panel: General, Plastic Surgery
Date received: 1990-12-24
Decision date: 1991-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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K933135 — DAWN DISPOSABLE BIOPSY FORCEPS1994-03-07
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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.