Nanma Mfg Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nanma Mfg Co., Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Nanma Mfg Co., Ltd. has 9 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 9 cleared submissions from 2000 to 2004. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nanma Mfg Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nanma Mfg Co., Ltd.
9 devices
Cleared
Aug 25, 2004
NANMA VACUUM PUMP PROXZEK MODEL 2M9498S
Gastroenterology & Urology
72d
Cleared
Aug 06, 2003
NANMA ADJUSTABLE CONSTRICTION RING
Gastroenterology & Urology
205d
Cleared
Jun 03, 2003
NANMA VACUUM PUMP
Gastroenterology & Urology
71d
Cleared
Dec 20, 2002
MODIFICATION TO NANMA VACUUM PUMP
Gastroenterology & Urology
458d
Cleared
Aug 22, 2002
NANMA ADJUSTABLE CONSTRICTION RING
Gastroenterology & Urology
345d
Cleared
May 09, 2002
MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING
Gastroenterology & Urology
240d
Cleared
Jul 19, 2000
NANMA VACUUM PUMP
Gastroenterology & Urology
245d
Cleared
Jan 31, 2000
NANMA NON-ADJUSTABLE CONSTRICTION RING
Gastroenterology & Urology
75d
Cleared
Jan 31, 2000
NANMA AJUSTABLE CONSTRICTION RING
Gastroenterology & Urology
75d