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FDA 510(k)

TECNOL ISLAND WOUND DRESSING

K-Number: K954033 · 1995-09-22

ApplicantTecnol Medical Products, Inc.
Decision Date1995-09-22
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

TECNOL ISLAND WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol Medical Products, Inc.. It received FDA 510(k) clearance on 1995-09-22 under 510(k) number K954033. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the TECNOL ISLAND WOUND DRESSING?

TECNOL ISLAND WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-09-22. The listed applicant is Tecnol Medical Products, Inc.. The 510(k) number is K954033.

When did TECNOL ISLAND WOUND DRESSING receive FDA 510(k) clearance?

TECNOL ISLAND WOUND DRESSING received FDA 510(k) clearance on 1995-09-22, under 510(k) number K954033.

Who is the listed applicant for TECNOL ISLAND WOUND DRESSING?

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

What is the FDA product code for TECNOL ISLAND WOUND DRESSING?

The FDA product code for TECNOL ISLAND WOUND DRESSING is MGP.

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Other records listing Tecnol 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.

K974068PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICAL MASK REGULAR SIZE, PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICALK970448PCM 2000; ISOLAIR APR MODEL 2735K963564PERSONAL LIMB HOLDER (24444-200,300,24444-KIT)K963559WRPAROUND LIMB HOLDER (24446,24446-350,24447-010,24449-010)K963552QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)K963556SECURE-ALL 1-PIECE BODY HOLDER, SMALL/MEDIUM (24451-010,020,24452-010,020,030)

View all 21 devices →

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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