Quest Intl., Inc.
Quest Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2009.
Top product codes for Quest Intl., Inc.
Recent clearances by Quest Intl., Inc.
- K091260 — SERAQUEST EBV EA-D IGG TEST
- K033915 — MODIFICATION TO SERAQUEST EB VCA IGG
- K033780 — MODIFICATION TO SERAQUEST VCA IGM
- K023593 — SERAQUEST ANTI-THYROID PEROXIDASE (TPO)
- K023592 — SERAQUEST ANTI-THYROGLOBULIN
- K003069 — ANTI-CARDIOLIPIN, MULTIPLE AUTOANTIBODIES IMMUNOLOGICAL TEST SYSTEM
- K991975 — SERAQUEST EB NA IGG
- K990410 — SERAQUEST EB VCA IGG
- K990977 — SERAQUEST EB VAC IGM
- K982485 — SERAQUEST CMV IGM
- K982281 — SERAQUEST RUBELLA IGM
- K980540 — SERAQUEST ANTI-SM
- K980639 — SERAQUEST ANTI-SSB
- K980810 — SERAQUEST ANTI-SSA
- K980811 — SERAQUEST ANTI-SM/RNP
- K980391 — SERAQUEST ANTI-DSDNA
- K980059 — SERAQUEST MUMPS IGG
- K972295 — SERAQUEST VZV IGG
- K971672 — SERAQUEST TOXOPLASMA IGM
- K963282 — SERAQUEST HSV IGG
- K961053 — SERAQUEST RUBELLA IGG
- K960092 — SERAQUEST TOXOPLASMA IGG
- K954191 — SERAQUEST CMV IGG
- K891736 — PATIENT EXAMINATION GLOVES (LATEX)
- K890356 — LATEX EXAMINATION GLOVES NON-STERILE
Data sourced from openFDA. This site is unofficial and independent of the FDA.