Medical Device Manufacturer · US , Mchenry , IL

Electro-Nucleonics Laboratories, Inc. - FDA 510(k) Cleared Devices

41 submissions · 41 cleared · Since 1976

Total

Cleared

Denied

Electro-Nucleonics Laboratories, Inc. has 41 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 41 cleared submissions from 1976 to 1988. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Electro-Nucleonics Laboratories, Inc. Filter by specialty or product code using the sidebar.

Electro-Nucleonics 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 - Electro-Nucleonics Laboratories, Inc.

41 devices

1-12 of 41

Cleared Feb 24, 1988

VIRGO(TM) MEASLES IGG ELISA

MULTI-ACCESS REAGENT DISPENSER

K873416 · JQW

Chemistry · 45d

Cleared Sep 11, 1987

GEMENI URIC ACID U.V.

K873358 · CDO

Chemistry · 21d

Cleared Sep 09, 1987

VIRGO(TM) RUBELLA IGG ELISA

K873088 · LFX

Microbiology · 35d

Cleared Jul 30, 1987

TOXOPLASMA GONDII IGG ELISA

K871905 · LGD

Microbiology · 76d

Cleared Apr 22, 1987

CHOLESTEROL (TOTAL) ANALYSIS PRODUCTS

K870928 · CHH

Chemistry · 44d

Cleared Nov 13, 1986

LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES

GEMSTAR IPA THEOPHYLLINE TEST KIT

GEMENI AST-LTS REAGENTS

K851267 · CIT

Chemistry · 31d

Looking for a specific device from Electro-Nucleonics...? Search by device name or K-number.

Search all Electro-Nucleonics... devices

Electro-Nucleonics Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Electro-Nucleonics Laboratories, Inc.

Filters