Bay Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bay Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EchoMD Automated Ejection Fraction Software
2
Total
1
Cleared
1
Denied
Bay Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Bay Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Bay Labs, Inc.
2 devices