LASERSKIN DRESSING— 510(k) K001508

Name: FDA 510(k) clearance K001508
Creator: U.S. Food and Drug Administration
Published: 2001-07-25

Substantially Equivalent

Fidia Advanced Biopolymers Srl

FDA 510(k) clearance K001508 for LASERSKIN DRESSING, Substantially Equivalent on 2001-07-25. Applicant: Fidia Advanced Biopolymers Srl. Device class: Unclassified.

Clearance details

Applicant: Fidia Advanced Biopolymers Srl
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 2000-05-15
Decision date: 2001-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abano Terme, IT

Download summary PDF View on FDA.gov ↗

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K012995 — COLLATEK SHEET2001-10-25
K012997 — COLLATEK FOAM2001-10-25
K990079 — FASTSEAL CHEST WOUND DRESSING1999-12-23
K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14
K992302 — DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS1999-09-14

More clearances from Fidia Advanced Biopolymers Srl

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Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.