MULTIPLE BIOPSY DEVICE-MBX— 510(k) K911448

Name: FDA 510(k) clearance K911448
Creator: U.S. Food and Drug Administration
Published: 1991-04-16

Substantially Equivalent

Triton Technology, Inc.

FDA 510(k) clearance K911448 for MULTIPLE BIOPSY DEVICE-MBX, Substantially Equivalent on 1991-04-16. 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: 1991-03-15
Decision date: 1991-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salem, OH, US

Download summary PDF View on FDA.gov ↗

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