MODIFICATION TO SKVEKPATCH— 510(k) K984177

Name: FDA 510(k) clearance K984177
Creator: U.S. Food and Drug Administration
Published: 1998-12-18

Substantially Equivalent for Some Indications

Marine Polymer Technologies, Inc.

FDA 510(k) clearance K984177 for MODIFICATION TO SKVEKPATCH, Substantially Equivalent for Some Indications on 1998-12-18. Applicant: Marine Polymer Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Marine Polymer Technologies, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1998-11-20
Decision date: 1998-12-18
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

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