510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K842222Unknown

Dupont Aca Liquid Bilirubin Calibrator

E.I. Dupont de Nemours & Co., Inc., Mchenry IL / Traditional, Unknown
FDA source (opens on fda.gov)

K842222 is the FDA 510(k) clearance record for DUPONT ACA LIQUID BILIRUBIN CALIBRATOR, cleared for E.I. Dupont DE Nemours & Co., Inc. on . FDA records list 253 510(k) clearances for E.I. Dupont DE Nemours & Co., Inc., from to . As of , FDA records show no recalls naming K842222.

Clearance record

Decision date
Received
(0 days to decision)
Review panel
Unknown
Applicant
E.I. Dupont DE Nemours & Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No