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FDA 510(k)

DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS

K-Number: K992302 · 1999-09-14

ApplicantDermaphylyx, Inc.
Decision Date1999-09-14
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Dermaphylyx, Inc.. It received FDA 510(k) clearance on 1999-09-14 under 510(k) number K992302. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS?

DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS is a medical device that received FDA 510(k) clearance on 1999-09-14. The listed applicant is Dermaphylyx, Inc.. The 510(k) number is K992302.

When did DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS receive FDA 510(k) clearance?

DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS received FDA 510(k) clearance on 1999-09-14, under 510(k) number K992302.

Who is the listed applicant for DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS?

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

What is the FDA product code for DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS?

The FDA product code for DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS is MGP.

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Other records listing Dermaphylyx, 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.

K991920DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSINGK991933DERMAPHYLYX FOAM ISLAND DRESSINGK991609DERMAPHYLYX SUPER ABSORBENT FIBER DRESSINGK991608DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSINGK991061DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSINGK990875DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND 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.K992005GILTECH PLUS TRANSPARENT DRESSINGGiltech Plus, 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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