Medical Device Manufacturer · US , Plainville , CT

Acme-Monaco Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Acme-Monaco Corp. Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Nov 18, 1988

ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH

Gastroenterology & Urology · 73d