PRESTITCH— 510(k) K910449

Name: FDA 510(k) clearance K910449
Creator: U.S. Food and Drug Administration
Published: 1992-05-29

Substantially Equivalent

Crantec Co.

FDA 510(k) clearance K910449 for PRESTITCH, Substantially Equivalent on 1992-05-29. Applicant: Crantec Co.. Device class: 1.

Clearance details

Applicant: Crantec Co.
Product code: Code KCY
Device class: Class 1
Regulation: 21 CFR 878.5910
Advisory panel: General, Plastic Surgery
Date received: 1991-01-29
Decision date: 1992-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KCY

product code KCY

Malfunction: 868
Total: 868

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.