MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES— 510(k) K884097

Name: FDA 510(k) clearance K884097
Creator: U.S. Food and Drug Administration
Published: 1989-04-17

Substantially Equivalent

Circon Acmi

FDA 510(k) clearance K884097 for MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES, Substantially Equivalent on 1989-04-17. Applicant: Circon Acmi. Device class: 2.

Clearance details

Applicant: Circon Acmi
Product code: Code ODC
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1988-09-28
Decision date: 1989-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stamford, CT, US

Download summary PDF View on FDA.gov ↗

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