Medical Device Manufacturer · CA , Ontario M5t 1x4

Cyberfluor, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1987

Total

Cleared

Denied

Cyberfluor, Inc. has 17 FDA 510(k) cleared chemistry devices. Based in Ontario M5t 1x4, CA.

Historical record: 17 cleared submissions from 1987 to 1992.

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

Cyberfluor, 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 - Cyberfluor, Inc.

17 devices

1-12 of 17

FLAGEN TRIIODOTHYRONINE (T3) ASSAY

FIAGEN T3 UPTAKE CATALOGUE #101-402

K895186 · KHQ

Chemistry · 89d

Cleared Oct 31, 1989

CYBERFLUOR FIAGEN TSH

K895396 · JLW

Toxicology · 60d

Cleared Jan 17, 1989

FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT

K884707 · LCS

Chemistry · 69d

Cleared Jan 17, 1989

FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KIT

K884708 · CGJ

Chemistry · 69d

Cleared Dec 14, 1988

FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT

FIAGEN HGH FLUOROIMMUNOASSAY KIT

Cyberfluor, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cyberfluor, Inc.

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