Medical Device Manufacturer · US , Medford , MA

Rowenta, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rowenta, Inc. Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Sep 23, 2003

ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620)

Gastroenterology & Urology · 347d