Immunoprobe, Inc.
Immunoprobe, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1997.
Top product codes for Immunoprobe, Inc.
Recent clearances by Immunoprobe, Inc.
- K972406 — ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM
- K971393 — MYCOPLASMA IGG ELISA TEST SYSTEM
- K961764 — PR-3 ELISA TEST SYSTEM
- K961765 — MPO ELISA TEST SYSTEM
- K951549 — EBNA IGG EIA TEST SYSTEM
- K952521 — CARDIOLIPIN IGM EIA TEST SYSTEM
- K952522 — CARDIOLIPIN IGA EIA TEST SYSTEM
- K952523 — CARDIOLIPIN IGG EIA TEST KIT
- K951362 — THYROGLOBULIN EIA TEST KIT
- K951364 — MICROSOMAL EIA TEST KIT
- K951363 — CARDIOLIPIN IGG,M,A EIA TEST SYSTEM
- K952520 — CARDIOLIPIN IGG,M,A EIA TEST KIT
- K941358 — THYROGLOBULIN EIA TEST KIT
- K941361 — MICROSOMAL EIA TEST KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.