Medical Device Manufacturer · US , Sandy , UT

Regulatory Consultants TO the Medical Device Indus - FDA 510(k) Clear...

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Regulatory Consultants TO the Medical Device Indus has 1 FDA 510(k) cleared medical devices. Based in Sandy, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Regulatory Consultants TO the Medical Device Indus Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Regulatory Consultants TO the Medical Device Indus

1 devices

1-1 of 1

Cleared Aug 09, 1994

ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES

K935157 · KPX

Radiology · 285d

Regulatory Consultants TO the Medical Device Indus - FDA 510(k) Clear...

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