Pro-Lab, Inc.
Pro-Lab, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1995.
Top product codes for Pro-Lab, Inc.
Recent clearances by Pro-Lab, Inc.
- K934383 — PROLEX (STREPTOCCAL GROUPING LATEX KIT)
- K914419 — AMNIOTEST(TM)
- K921421 — LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY
- K903714 — E. COLI 0157 LATEX TEST
- K894221 — ROSCO PYRR
- K883995 — X-ACT UREA/TDA
- K883996 — X-ACT LDC/IND
- K871121 — PROTECT T.M.
- K870117 — NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST
- K861142 — MASTER KIT B
- K861888 — HIPPURATE HYDROLYSIS TEST
- K861889 — D'ALA RAPID TEST
- K850246 — MASTER KIT A
- K850302 — SUPLEX & SUPLEX DILUENT
- K850299 — C.N.V.T.
- K850300 — MUCOLYSE
- K850301 — YEAST DIALYSATE
- K850306 — CAMPYLOBACTER SUPPLEMENT -SKIRROW
- K850307 — CAMPYLOBACTER SUPPLEMENT-BLASER/WANG
- K850308 — C.L.A.T.
- K850072 — CUSTOM OPEN HEART TRAY
- K843813 — INTRAVENOUS START KIT
- K842404 — DRESSING CHANGE TRAY STERILE 5002
- K843627 — VENESECTION TRAY, ADULT 6050
- K843525 — SUTURE TRAY
- K843982 — O.B. BASIN SET
- K842405 — DR. GOULD HAND PACK SUSTOM STERIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.