SPYROSORB FOAM ISLAND WOUND DRESSING— 510(k) K980673

Name: FDA 510(k) clearance K980673
Creator: U.S. Food and Drug Administration
Published: 1998-05-21

Substantially Equivalent for Some Indications

Innovative Technologies (Us), Inc.

FDA 510(k) clearance K980673 for SPYROSORB FOAM ISLAND WOUND DRESSING, Substantially Equivalent for Some Indications on 1998-05-21. Applicant: Innovative Technologies (Us), Inc.. Device class: 1.

Clearance details

Applicant: Innovative Technologies (Us), Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1998-02-20
Decision date: 1998-05-21
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Golden,, CO, US

Download summary PDF View on FDA.gov ↗

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