Medical Device Manufacturer · US , Mchenry , IL

E-Y Laboratories, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1983

Total

Cleared

Denied

E-Y Laboratories, Inc. has 13 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1983 to 1994.

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

E-Y Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - E-Y Laboratories, Inc.

13 devices

1-13 of 13

GONOCHEK-II, MODIFICATION

K934125 · JTO

Microbiology · 393d

Cleared Sep 09, 1994

B-LACTAMASE REAGENT TUBES

K940161 · JTO

Microbiology · 240d

Cleared Sep 09, 1994

GONOCHEK II REAGENT TUBES

STREP-A-CHEK(TM) REAGENT STRIPS

E-Y Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - E-Y Laboratories, Inc.

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