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FDA 510(k)

BIO-DRESSING, STERILE ISLAND DRESSING

K-Number: K961098 · 1996-05-03

ApplicantK. W. Griffen Co.
Decision Date1996-05-03
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

BIO-DRESSING, STERILE ISLAND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is K. W. Griffen Co.. It received FDA 510(k) clearance on 1996-05-03 under 510(k) number K961098. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BIO-DRESSING, STERILE ISLAND DRESSING?

BIO-DRESSING, STERILE ISLAND DRESSING is a medical device that received FDA 510(k) clearance on 1996-05-03. The listed applicant is K. W. Griffen Co.. The 510(k) number is K961098.

When did BIO-DRESSING, STERILE ISLAND DRESSING receive FDA 510(k) clearance?

BIO-DRESSING, STERILE ISLAND DRESSING received FDA 510(k) clearance on 1996-05-03, under 510(k) number K961098.

Who is the listed applicant for BIO-DRESSING, STERILE ISLAND DRESSING?

The FDA 510(k) record lists K. W. Griffen Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-DRESSING, STERILE ISLAND DRESSING?

The FDA product code for BIO-DRESSING, STERILE ISLAND DRESSING 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 K. W. Griffen 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.

K953810FLUFF GAUZE BANDAGE, STERILE & NON-STERILEK874161MODIFIED USE OF TRIANGLE BANDAGE STERILEK870258BIOSCRUB SURGICAL SCRUB BRUSH

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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