CUTIFILM(R) FILM— 510(k) K926399

Name: FDA 510(k) clearance K926399
Creator: U.S. Food and Drug Administration
Published: 1993-11-15

Substantially Equivalent

Beiersdorf, Inc.

FDA 510(k) clearance K926399 for CUTIFILM(R) FILM, Substantially Equivalent on 1993-11-15. Applicant: Beiersdorf, Inc.. Device class: Unclassified.

Clearance details

Applicant: Beiersdorf, Inc.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-12-21
Decision date: 1993-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

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K952526 — CUTINOVA CAVITY1995-08-14
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Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

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.