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FDA 510(k)

EPIVIEW

K-Number: K940895 · 1994-11-22

ApplicantConvatec, A Bristol-Myers Squibb Co.
Decision Date1994-11-22
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

EPIVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Bristol-Myers Squibb Co.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K940895. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the EPIVIEW?

EPIVIEW is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Convatec, A Bristol-Myers Squibb Co.. The 510(k) number is K940895.

When did EPIVIEW receive FDA 510(k) clearance?

EPIVIEW received FDA 510(k) clearance on 1994-11-22, under 510(k) number K940895.

Who is the listed applicant for EPIVIEW?

The FDA 510(k) record lists Convatec, A Bristol-Myers Squibb Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPIVIEW?

The FDA product code for EPIVIEW is MGP.

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Other records listing Convatec, A Bristol-Myers Squibb Co. 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.

K032734CONVATEC FECAL MANAGEMENT SYSTEMK990368DUODERM HYDROACTIVE GEL WOUND DRESSINGK982116AQUACEL HYDROFIBER WOUND DRESSINGK973806DUODERM HYDROACTIVE GELK973807DUODERM HYDROACTIVE PASTEK973717COMBIDERM ACD

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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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