NANMA ADJUSTABLE CONSTRICTION RING— 510(k) K013051

Name: FDA 510(k) clearance K013051
Creator: U.S. Food and Drug Administration
Published: 2002-08-22

Substantially Equivalent

Nanma Mfg Co., Ltd.

FDA 510(k) clearance K013051 for NANMA ADJUSTABLE CONSTRICTION RING, Substantially Equivalent on 2002-08-22. 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: 2001-09-11
Decision date: 2002-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKY

view all

K041573 — NANMA VACUUM PUMP PROXZEK MODEL 2M9498S2004-08-25
K032776 — VACURECT VACUUM CONSTRICTION DEVICE2003-10-03
K030119 — NANMA ADJUSTABLE CONSTRICTION RING2003-08-06
K030913 — NANMA VACUUM PUMP2003-06-03
K013113 — MODIFICATION TO NANMA VACUUM PUMP2002-12-20

More clearances from Nanma Mfg Co., Ltd.

view all

K013053 — MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING2002-05-09
K993909 — NANMA VACUUM PUMP2000-07-19
K993906 — NANMA NON-ADJUSTABLE CONSTRICTION RING2000-01-31
K993908 — NANMA AJUSTABLE CONSTRICTION RING2000-01-31

Data sourced from openFDA. This site is unofficial and independent of the FDA.