MANAN UBK ULTRASONIC GUIDED BIOPSY KIT— 510(k) K852105

Name: FDA 510(k) clearance K852105
Creator: U.S. Food and Drug Administration
Published: 1985-06-18

Unknown

Manan Manufacturing Co., Inc.

FDA 510(k) clearance K852105 for MANAN UBK ULTRASONIC GUIDED BIOPSY KIT, Unknown on 1985-06-18. Applicant: Manan Manufacturing Co., Inc.. Device class: 1.

Clearance details

Applicant: Manan Manufacturing Co., Inc.
Product code: Code FCH
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1985-05-15
Decision date: 1985-06-18
Decision: Unknown
Clearance type: Traditional
Location: Skokie, IL, US

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