510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834472Substantially Equivalent

Deseret Epidural Catheter

Parke-Davis Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834472 is the FDA 510(k) clearance record for DESERET EPIDURAL CATHETER, cleared for Parke-Davis Co. on . FDA records list 47 510(k) clearances for Parke-Davis Co., from to . As of , FDA records show no recalls naming K834472.

Clearance record

Decision date
Received
(24 days to decision)
Review panel
Unknown
Applicant
Parke-Davis Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No