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FDA 510(k)

LASERSKIN DRESSING

K-Number: K001508 · 2001-07-25

ApplicantFidia Advanced Biopolymers Srl
Decision Date2001-07-25
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

LASERSKIN DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Fidia Advanced Biopolymers Srl. It received FDA 510(k) clearance on 2001-07-25 under 510(k) number K001508. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERSKIN DRESSING?

LASERSKIN DRESSING is a medical device that received FDA 510(k) clearance on 2001-07-25. The listed applicant is Fidia Advanced Biopolymers Srl. The 510(k) number is K001508.

When did LASERSKIN DRESSING receive FDA 510(k) clearance?

LASERSKIN DRESSING received FDA 510(k) clearance on 2001-07-25, under 510(k) number K001508.

Who is the listed applicant for LASERSKIN DRESSING?

The FDA 510(k) record lists Fidia Advanced Biopolymers Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASERSKIN DRESSING?

The FDA product code for LASERSKIN 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 Fidia Advanced Biopolymers Srl 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.

K092257JALOSKINK073251HYALOMATRIX PAK003855HYALOMATRIX CO

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.

K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, Inc.K992005GILTECH PLUS TRANSPARENT DRESSINGGiltech Plus, 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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