Medical Device Manufacturer · US , New York , NY

Isratech Marketing Corp.

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Isratech Marketing Corp. — FDA 510(k) Submissions

Isratech Marketing Corp. has submitted 2 FDA 510(k) premarket notifications since 1987, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dish, Tissue Culture, Surgeon's Gloves . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

STERILE HYPOALLERGENIC SURGEONS' GLOVES

K896165 · KGO Surgeon's Gloves · General Hospital

Nov 1989 28d

TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES

K871483 · KIZ Dish, Tissue Culture · Pathology

Apr 1987 14d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Isratech Marketing Corp.

Isratech Marketing Corp. — FDA 510(k) Submissions

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