SUCTION GUILLOTINE DEVICE— 510(k) K932142

Name: FDA 510(k) clearance K932142
Creator: U.S. Food and Drug Administration
Published: 1993-09-24

Substantially Equivalent

Triton Technology, Inc.

FDA 510(k) clearance K932142 for SUCTION GUILLOTINE DEVICE, Substantially Equivalent on 1993-09-24. Applicant: Triton Technology, Inc.. Device class: 2.

Clearance details

Applicant: Triton Technology, Inc.
Product code: Code FCK
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 1993-05-03
Decision date: 1993-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salem, OH, US

Download summary PDF View on FDA.gov ↗

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