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FDA 510(k)

CUTIFILM(R) FILM

K-Number: K926399 · 1993-11-15

ApplicantBeiersdorf, Inc.
Decision Date1993-11-15
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

CUTIFILM(R) FILM is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1993-11-15 under 510(k) number K926399. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTIFILM(R) FILM?

CUTIFILM(R) FILM is a medical device that received FDA 510(k) clearance on 1993-11-15. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K926399.

When did CUTIFILM(R) FILM receive FDA 510(k) clearance?

CUTIFILM(R) FILM received FDA 510(k) clearance on 1993-11-15, under 510(k) number K926399.

Who is the listed applicant for CUTIFILM(R) FILM?

The FDA 510(k) record lists Beiersdorf, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUTIFILM(R) FILM?

The FDA product code for CUTIFILM(R) FILM is MGP.

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Other records listing Beiersdorf, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MGP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K001508LASERSKIN DRESSINGFidia Advanced Biopolymers SrlK990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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