B&B Medical Assoc., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
B&B Medical Assoc., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
B&B Medical Assoc., Inc. has 5 FDA 510(k) cleared medical devices. Based in Danvers, US.
Historical record: 5 cleared submissions from 1988 to 1988. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by B&B Medical Assoc., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - B&B Medical Assoc., Inc.
5 devices
Cleared
Oct 21, 1988
INTROCULAR FLUID INJECTOR
Gastroenterology & Urology
193d
Cleared
Sep 08, 1988
VAC-G (GUILLOTINE VITRECTOR)
Ophthalmic
150d
Cleared
Sep 07, 1988
VAC (OSCILLATING VITRECTOR)
Ophthalmic
149d
Cleared
Aug 22, 1988
B & B I/A HANDPIECE
Ophthalmic
133d
Cleared
Aug 22, 1988
INFUSION HANDLE
Ophthalmic
133d