Medical Device Manufacturer · US , New York , NY

Isratech Marketing Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987
2
Total
2
Cleared
0
Denied

Isratech Marketing Corp. has 2 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 2 cleared submissions from 1987 to 1989. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Isratech Marketing Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Isratech Marketing Corp.
2 devices
1-2 of 2
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