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FDA 510(k)

GILTECH PLUS TRANSPARENT DRESSING

K-Number: K992005 · 1999-09-03

ApplicantGiltech Plus, Inc.
Decision Date1999-09-03
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

GILTECH PLUS TRANSPARENT DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Giltech Plus, Inc.. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K992005. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GILTECH PLUS TRANSPARENT DRESSING?

GILTECH PLUS TRANSPARENT DRESSING is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Giltech Plus, Inc.. The 510(k) number is K992005.

When did GILTECH PLUS TRANSPARENT DRESSING receive FDA 510(k) clearance?

GILTECH PLUS TRANSPARENT DRESSING received FDA 510(k) clearance on 1999-09-03, under 510(k) number K992005.

Who is the listed applicant for GILTECH PLUS TRANSPARENT DRESSING?

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

What is the FDA product code for GILTECH PLUS TRANSPARENT DRESSING?

The FDA product code for GILTECH PLUS TRANSPARENT 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.

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Other records listing Giltech Plus, 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.

K992094GILTECH PLUS HYDROGEL SKIN DRESSINGK983624GILTECH PLUS CONNECTING TUBE SET

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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