MULTIPLE BIOPSY DEVICE-MBX— 510(k) K911448

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..

Clearance details

Applicant: Triton Technology, Inc.
Product code: Code FCK
Advisory panel: Gastroenterology, Urology
Date received: 1991-03-15
Decision date: 1991-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salem, OH, US

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