Medical Device Manufacturer · US , Mchenry , IL

Remel Co. - FDA 510(k) Cleared Devices

137 submissions · 137 cleared · Since 1979

137

Total

137

Cleared

Denied

Remel Co. has 137 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 137 cleared submissions from 1979 to 2001.

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

FDA 510(k) Regulatory Record - Remel Co.

137 devices

1-12 of 137

1 2 3 4

CALCOFLUOR WHITE STAIN KIT

K960090 · JTS

Microbiology · 68d

Cleared Mar 19, 1996

BACTIDROP CALCOFLUOR WHITE

K960095 · JTS

Microbiology · 68d

Cleared Feb 23, 1996

REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK

BHI AGAR WITH VANCOMYCIN

RIM E.COLI 0157:H7 LATEX TEST

K933457 · GNA

Microbiology · 280d

1 2 3 4

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Remel Co. - FDA 510(k) Cleared Devices

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