Cypris eXact Suture Placement Device— 510(k) K240185

Name: FDA 510(k) clearance K240185
Creator: U.S. Food and Drug Administration
Published: 2024-05-03

Substantially Equivalent

Cypris Medical

FDA 510(k) clearance K240185 for Cypris eXact Suture Placement Device, Substantially Equivalent on 2024-05-03. Applicant: Cypris Medical. Device class: 1.

Clearance details

Applicant: Cypris Medical
Product code: Code GEJ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 2024-01-23
Decision date: 2024-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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