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FDA 510(k)

SIMPLICARE THIN FILM WOUND DRESSINGS

K-Number: K980209 · 1998-02-20

ApplicantHollister, Inc.
Decision Date1998-02-20
Product CodeMGP
DecisionUnknown

Device Summary

SIMPLICARE THIN FILM WOUND DRESSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1998-02-20 under 510(k) number K980209. The device is classified under product code MGP. FDA Decision: Unknown.

Frequently Asked Questions

What is the SIMPLICARE THIN FILM WOUND DRESSINGS?

SIMPLICARE THIN FILM WOUND DRESSINGS is a medical device that received FDA 510(k) clearance on 1998-02-20. The listed applicant is Hollister, Inc.. The 510(k) number is K980209.

When did SIMPLICARE THIN FILM WOUND DRESSINGS receive FDA 510(k) clearance?

SIMPLICARE THIN FILM WOUND DRESSINGS received FDA 510(k) clearance on 1998-02-20, under 510(k) number K980209.

Who is the listed applicant for SIMPLICARE THIN FILM WOUND DRESSINGS?

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

What is the FDA product code for SIMPLICARE THIN FILM WOUND DRESSINGS?

The FDA product code for SIMPLICARE THIN FILM WOUND DRESSINGS is MGP.

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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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