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FDA 510(k)

BIODERM MEDICAL TRANSPARENT FILM DRESSING

K-Number: K951842 · 1995-06-12

ApplicantBioderm, Inc.
Decision Date1995-06-12
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

BIODERM MEDICAL TRANSPARENT FILM DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Bioderm, Inc.. It received FDA 510(k) clearance on 1995-06-12 under 510(k) number K951842. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIODERM MEDICAL TRANSPARENT FILM DRESSING?

BIODERM MEDICAL TRANSPARENT FILM DRESSING is a medical device that received FDA 510(k) clearance on 1995-06-12. The listed applicant is Bioderm, Inc.. The 510(k) number is K951842.

When did BIODERM MEDICAL TRANSPARENT FILM DRESSING receive FDA 510(k) clearance?

BIODERM MEDICAL TRANSPARENT FILM DRESSING received FDA 510(k) clearance on 1995-06-12, under 510(k) number K951842.

Who is the listed applicant for BIODERM MEDICAL TRANSPARENT FILM DRESSING?

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

What is the FDA product code for BIODERM MEDICAL TRANSPARENT FILM DRESSING?

The FDA product code for BIODERM MEDICAL TRANSPARENT FILM DRESSING is MGP.

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Other records listing Bioderm, 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.

K990955MODIFICATION OF:BIODERM FOAM WOUND DRESSINGK982778BIODERM FOAM WOUND DRESSINGK982939BTF THIN FILM WOUND DRESSINGK980451BIODERM CALCIUM ALGINATE DRESSINGK973429BIODERM FOAM WOUND DRESSINGK963950BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE

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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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