LACERATION TRAY— 510(k) K932036

Name: FDA 510(k) clearance K932036
Creator: U.S. Food and Drug Administration
Published: 1993-12-13

Unknown

Clinipad Corp.

FDA 510(k) clearance K932036 for LACERATION TRAY, Unknown on 1993-12-13. Applicant: Clinipad Corp.. Device class: 2.

Clearance details

Applicant: Clinipad Corp.
Product code: Code FRG
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 1993-04-27
Decision date: 1993-12-13
Decision: Unknown
Clearance type: Traditional
Location: Guilford, CT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

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.