510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K813220Substantially Equivalent

Regu-Vac Oxygenating Suction Catheter

BD Becton Dickinson Vacutainer Systems Preanalytic, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K813220 is the FDA 510(k) clearance record for REGU-VAC OXYGENATING SUCTION CATHETER, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on . FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K813220.

Clearance record

Decision date
Received
(74 days to decision)
Review panel
Unknown
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 1875 Eye St. NW Suite 625, Washington DC
Third party review
No