Medical Device Manufacturer · US , Rockville , MD

Immuno-U.S., Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997
1
Total
1
Cleared
0
Denied

Immuno-U.S., Inc. has 1 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Immuno-U.S., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Immuno-U.S., Inc.

1 devices
1-1 of 1
Cleared Dec 08, 1997
DUPLOJECT (0.5/1.0 ML, 2.0 ML, 5.0 ML)
K973510 · FMF
General Hospital · 83d
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