Beiersdorf, Inc. - FDA 510(k) Cleared Devices
45
Total
39
Cleared
0
Denied
FDA 510(k) Regulatory Record - Beiersdorf, Inc. Gastroenterology & Urology ✕
4 devices
Cleared
Oct 07, 1994
NORTA
Gastroenterology & Urology
318d
Cleared
Apr 01, 1987
NORTA (TM) UROBAG
Gastroenterology & Urology
56d
Cleared
Apr 08, 1986
NORTA TEFLON COATED LATEX BALLOON CATHETERS
Gastroenterology & Urology
8d
Cleared
Nov 21, 1984
NORTA SILICONIZED LATEX BALLOON CATH.
Gastroenterology & Urology
154d