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FDA 510(k)

CUTIPLAST STERIL

K-Number: K943363 · 1995-03-15

ApplicantBeiersdorf, Inc.
Decision Date1995-03-15
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

CUTIPLAST STERIL is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1995-03-15 under 510(k) number K943363. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTIPLAST STERIL?

CUTIPLAST STERIL is a medical device that received FDA 510(k) clearance on 1995-03-15. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K943363.

When did CUTIPLAST STERIL receive FDA 510(k) clearance?

CUTIPLAST STERIL received FDA 510(k) clearance on 1995-03-15, under 510(k) number K943363.

Who is the listed applicant for CUTIPLAST STERIL?

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 CUTIPLAST STERIL?

The FDA product code for CUTIPLAST STERIL 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.

K090921ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02K024057CURAD SCAR THERAPYK952526CUTINOVA CAVITYK944581CUTINOVA THIN WOUND DRESSINGK935630NORTAK940378COVERLET ADHESIVE DRESSING

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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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