Medical Device Manufacturer · US , Columbia , MD

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

9 submissions · 9 cleared · Since 1988

Total

Cleared

Denied

Electro-Nucleonics, Inc. has 9 FDA 510(k) cleared medical devices. Based in Columbia, US.

Historical record: 9 cleared submissions from 1988 to 1989. Primary specialty: Microbiology.

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

Electro-Nucleonics, 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, Inc.

9 devices

1-9 of 9

Cleared Sep 28, 1989

DELTATEST (R) LIPASE II

K893718 · CET

Chemistry · 134d

Cleared Apr 28, 1989

SEROLOGICAL TEST KIT FOR IGG ANTI. EPSTEIN-BARR VI

K883670 · GNP

Microbiology · 253d

Cleared Mar 10, 1989

VIRGO HSV-2 IGG ELISA

K883281 · GQO

Microbiology · 219d

Cleared Mar 10, 1989

VIRGO HSV-1 IGG ELISA

K883282 · GQO

Microbiology · 219d

Cleared Mar 10, 1989

VIRGO(R) VZV-IGG ELISA

K883427 · GQX

Microbiology · 207d

Cleared Feb 08, 1989

VIRGO (R) CMV-IGG ELISA

K883102 · GQI

Microbiology · 201d

Cleared Dec 29, 1988

VIRGO(R) MICROWELL ALT ASSAY

K884784 · CKD

Chemistry · 44d

Cleared Sep 09, 1988

ALTLTS ALANINE AMINO TRANSFERASE ALT

K883205 · CKA

Chemistry · 43d

Cleared Sep 09, 1988

LACTATE DEHYDROGENASE LDH

K883206 · CFJ

Chemistry · 43d

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

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

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