Wallac OY
Wallac OY holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2014, with 1 FDA device recall on record.
Top product codes for Wallac OY
FDA recalls by Wallac OY
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Wallac OY
- DEN140010 — PERKINELMER ENLITE NEONATAL TREC TEST SYSTEM
- K131284 — GSP NEONATAL BIOTINIDASE KIT
- K100682 — GSP NEONATAL 17A-OH-PROGESTERONE KIT MODEL: 3305-001U
- K081922 — AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
- K071649 — NEONATAL TOTAL GALACTOSE KIT; NEONTAL TOTAL GALACTOSE KIT, MODELS 3029-0010 AND 3029-110B
- K070889 — AUTODELFIA NEONATAL IRT L KIT, MODEL B022-112
- K050709 — RESOLVE HEMOGLOBIN KIT, JB-2 STAINING SYSTEM, MODELS FR-9120, FR-9400, FR-9360, FR-9367
- K050960 — MODIFICATION TO: AUTODELFIA NEONATAL 17A-OH-PROGESTERONE L KIT
- K042424 — DELFIA NEONATAL 17A-OH-PROGESTERONE KIT
- K042425 — AUTODELFIA NEONATAL 17A-OH-PROGESTERONE KIT
- K003664 — DELFIA NEONATAL IRT KIT, MODEL A005-110
- K003668 — AUTODELFIA NEONATAL IRT KIT, MODEL B005-112
- K993697 — DELFIA NEONATAL IRT KIT
- K943416 — DELFIA NEONATAL THYROXINE KIT
- K944490 — AUTODELFIA UNCONJUGATED ESTRIOL (UE3) KIT
- K940449 — DELFIA SHBG KIT
- K935047 — AUTO DELFIA
- K932951 — DELFIA TESTTOSTERONE KIT
- K930732 — DELFIA CORTISOL KIT
- K930484 — DELFIA(R) HGH KIT
- K924594 — DELFIA DIGOXIN KIT
- K923401 — DELFIA HTSH ULTRA KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.