510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K841300Substantially Equivalent

Antrum Needle-Wolf Type

Popper & Sons, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K841300 is the FDA 510(k) clearance record for ANTRUM NEEDLE-WOLF TYPE, cleared for Popper & Sons, Inc. on . FDA records list 8 510(k) clearances for Popper & Sons, Inc., from to . As of , FDA records show no recalls naming K841300.

Clearance record

Decision date
Received
(67 days to decision)
Review panel
Unknown
Applicant
Popper & Sons, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No