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
K850320Substantially Equivalent

Nebulizer Treatment Kit

Dhd Medical Products Div. Diemolding Corp., Canastota NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850320 is the FDA 510(k) clearance record for NEBULIZER TREATMENT KIT, cleared for Dhd Medical Products Div. Diemolding Corp. on . FDA records list 43 510(k) clearances for Dhd Medical Products Div. Diemolding Corp., from to . As of , FDA records show no recalls naming K850320.

Clearance record

Decision date
Received
(36 days to decision)
Review panel
Unknown
Applicant
Dhd Medical Products Div. Diemolding Corp. Division Of Diemolding Corp., Canastota NY
Third party review
No