Zip 4 Skin Closure Device— 510(k) K170003

Name: FDA 510(k) clearance K170003
Creator: U.S. Food and Drug Administration
Published: 2017-08-18

Substantially Equivalent

Zipline Medical, Inc.

FDA 510(k) clearance K170003 for Zip 4 Skin Closure Device, Substantially Equivalent on 2017-08-18. Applicant: Zipline Medical, Inc.. Device class: 1.

Clearance details

Applicant: Zipline Medical, Inc.
Product code: Code PYO
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 2017-01-03
Decision date: 2017-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Campbell, CA, US

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