Medical Device Manufacturer · CA , Quebec, Canada H7n4z9

I.A.F. Production, Inc. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1986

Total

Cleared

Denied

I.A.F. Production, Inc. has 29 FDA 510(k) cleared microbiology devices. Based in Quebec, Canada H7n4z9, CA.

Historical record: 29 cleared submissions from 1986 to 1987.

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

I.A.F. Production, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - I.A.F. Production, Inc.

29 devices

1-12 of 29

Cleared Sep 14, 1987

IAFP V. AGAR SELECTIVE

IAFP BILE ESCULIN AZIDE AGAR

K872672 · JSI

Microbiology · 35d

Cleared Aug 11, 1987

I.A.F.P. C.D.C. ANAEROBIC SHEEP BLOOD AGAR W/P.E.A

K872673 · JSJ

Microbiology · 35d

Cleared Aug 11, 1987

IAFP COLUMBIA C.N.A. WITH 5% SHEEP BLOOD

AFP MIDDLEBROOK 7H10 AGAR SLANT

K872676 · JSJ

Microbiology · 35d

Cleared Aug 11, 1987

IAFP HEKTOEN ENTERIC AGAR

K872680 · JSJ

Microbiology · 35d

Cleared Aug 11, 1987

IAFP C.D.C. ANAEROBIC AGAR W/5% SHEEP BLOOD

IAFP BILE ESCULIN AGAR

K872683 · JSI

Microbiology · 35d

I.A.F. Production, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - I.A.F. Production, Inc.

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