510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K842549Substantially Equivalent

Aca Acetaminophen Calibrator

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

K842549 is the FDA 510(k) clearance record for ACA ACETAMINOPHEN 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 K842549.

Clearance record

Decision date
Received
(45 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