Medical Device Manufacturer · US , San Jose , CA

Saratoga Intl., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Saratoga Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.

Historical record: 2 cleared submissions from 1990 to 1994. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Saratoga Intl., Inc. Filter by specialty or product code using the sidebar.

Saratoga Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Saratoga Intl., Inc.

2 devices

1-2 of 2