MODIFICATION TO NANMA VACUUM PUMP— 510(k) K013113

Name: FDA 510(k) clearance K013113
Creator: U.S. Food and Drug Administration
Published: 2002-12-20

Substantially Equivalent

Nanma Mfg Co., Ltd.

FDA 510(k) clearance K013113 for MODIFICATION TO NANMA VACUUM PUMP, Substantially Equivalent on 2002-12-20. Applicant: Nanma Mfg Co., Ltd.. Device class: 2.

Clearance details

Applicant: Nanma Mfg Co., Ltd.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 2001-09-18
Decision date: 2002-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

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