Medical Device Manufacturer · US , Fort Smith , AR

Quest Intl., Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 1989

Total

Cleared

Denied

Quest Intl., Inc. has 25 FDA 510(k) cleared medical devices. Based in Fort Smith, US.

Historical record: 25 cleared submissions from 1989 to 2009. Primary specialty: Microbiology.

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

Quest Intl., 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 - Quest Intl., Inc.

25 devices

1-25 of 25

Cleared Jun 08, 2009

SERAQUEST EBV EA-D IGG TEST

K091260 · LSE

Microbiology · 40d

Cleared Jan 16, 2004

MODIFICATION TO SERAQUEST EB VCA IGG

K033915 · LSE

Microbiology · 29d

Cleared Jan 15, 2004

MODIFICATION TO SERAQUEST VCA IGM

K033780 · LJN

Microbiology · 42d

Cleared Feb 06, 2003

SERAQUEST ANTI-THYROID PEROXIDASE (TPO)

K023593 · JZO

Immunology · 104d

Cleared Jan 06, 2003

SERAQUEST ANTI-THYROGLOBULIN

K023592 · DDC

Immunology · 73d

Cleared Nov 27, 2000

ANTI-CARDIOLIPIN, MULTIPLE AUTOANTIBODIES IMMUNOLOGICAL TEST SYSTEM

SERAQUEST RUBELLA IGM

SERAQUEST ANTI-SM/RNP

SERAQUEST TOXOPLASMA IGM

SERAQUEST RUBELLA IGG

K961053 · LFX

Microbiology · 170d

Cleared Jun 17, 1996

SERAQUEST TOXOPLASMA IGG

PATIENT EXAMINATION GLOVES (LATEX)

K891736 · LYY

General Hospital · 64d

Cleared Apr 06, 1989

LATEX EXAMINATION GLOVES NON-STERILE

K890356 · LYY

General Hospital · 72d

Quest Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Quest Intl., Inc.

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