The Boston & Pacific Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Boston & Pacific Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
The Boston & Pacific Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Hingham, US.
Historical record: 4 cleared submissions from 1990 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Boston & Pacific Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Boston & Pacific Co., Inc.
4 devices
Cleared
Feb 26, 1990
4 SURE EXTERNAL MALE CATHETER
Gastroenterology & Urology
89d
Cleared
Feb 20, 1990
4 SURE URINARY DRAIN BAG
Gastroenterology & Urology
83d
Cleared
Feb 20, 1990
4 SURE URINARY LEG BAG
Gastroenterology & Urology
83d
Cleared
Feb 16, 1990
4 SURE UROLOGICAL CATHETER
Gastroenterology & Urology
79d