SIGMA 1 WOBBLER BIOPSY KIT— 510(k) K882673

Name: FDA 510(k) clearance K882673
Creator: U.S. Food and Drug Administration
Published: 1988-07-28

Substantially Equivalent

Kontron Instruments, Inc.

FDA 510(k) clearance K882673 for SIGMA 1 WOBBLER BIOPSY KIT, Substantially Equivalent on 1988-07-28. Applicant: Kontron Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Kontron Instruments, Inc.
Product code: Code FCH
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1988-06-28
Decision date: 1988-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Everett, MA, US

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