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FDA 510(k)

DERM-A-TEC SKIN BARRIER FILM

K-Number: K822713 · 1982-12-07

ApplicantProfessional Medical Products, Inc.
Decision Date1982-12-07
Product Code
DecisionSubstantially Equivalent

Device Summary

DERM-A-TEC SKIN BARRIER FILM is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Products, Inc.. It received FDA 510(k) clearance on 1982-12-07 under 510(k) number K822713. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERM-A-TEC SKIN BARRIER FILM?

DERM-A-TEC SKIN BARRIER FILM is a medical device that received FDA 510(k) clearance on 1982-12-07. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K822713.

When did DERM-A-TEC SKIN BARRIER FILM receive FDA 510(k) clearance?

DERM-A-TEC SKIN BARRIER FILM received FDA 510(k) clearance on 1982-12-07, under 510(k) number K822713.

Who is the listed applicant for DERM-A-TEC SKIN BARRIER FILM?

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

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Other records listing Professional Medical Products, 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.

K926280STANDARD NEBULIZER HEATERK930270PATIENT PREOPERATIVE PREP TRAY, SINGLE USEK920292VARIOUS KITS AND TRAYSK862010CHICK SURGICAL LIGHTK860739CHICK SURIGICAL LIGHTK834478CHICK/REISON PATIENT EMERG. TROLLEY

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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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