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FDA 510(k)

TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING

K-Number: K952449 · 1995-08-07

ApplicantMedical Device Development Co.
Decision Date1995-08-07
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Development Co.. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K952449. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING?

TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Medical Device Development Co.. The 510(k) number is K952449.

When did TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING receive FDA 510(k) clearance?

TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING received FDA 510(k) clearance on 1995-08-07, under 510(k) number K952449.

Who is the listed applicant for TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING?

The FDA 510(k) record lists Medical Device Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING?

The FDA product code for TRANSAN, TRANSPARENT FILM DRESSING, TRANSPARENT WOUND DRSSING is MGP.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Device Development 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.

K952547COVERSAN, ISLESAN

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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