Barbaras Development, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Barbaras Development, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 0184 CO2 Sampling line
1
Total
1
Cleared
0
Denied
Barbaras Development, Inc. is a medical device manufacturer with a manufacturing facility in Newbury Park, US. The company specializes in product development, design, tooling, and manufacturing services across multiple industries.
The company has received 1 FDA 510(k) clearance from 1 total submission. Barbaras Development focuses exclusively on Anesthesiology devices, with its first and latest clearance both occurring in 2025. The company remains active in FDA regulatory submissions.
Explore the company's cleared device names, product codes, and clearance dates in the database above.
510(k) submissions have been managed by ProMedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Barbaras Development, Inc.
1 devices