Medical Device Manufacturer · US , Mchenry , IL

Monobind - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1977

Recent clearances: ACCUBIND NEONATAL T4 MICROPLATE EIA, MODEL 2625-300, FREE T4 (THYTOXINE) MICROPLATE EIA TEST MODELS # 1225-300, T-UPTAKE MICROPLATE EIA

21
Total
21
Cleared
0
Denied

Monobind has 21 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1977 to 2003.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Monobind

21 devices
1-12 of 21
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