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
K810029Unknown

Regulator Venoset W/0.22 Micron Ivex

Abbott Medical, Abbott Park IL / Traditional, Unknown
FDA source (opens on fda.gov)

K810029 is the FDA 510(k) clearance record for REGULATOR VENOSET W/0.22 MICRON IVEX, cleared for Abbott Laboratories on . FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K810029.

Clearance record

Decision date
Received
(0 days to decision)
Review panel
Unknown
Applicant
Abbott Laboratories One Abbott Park Rd., Abbott Park IL
Third party review
No