Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K844458Substantially Equivalent

Nd:yag Laser Pulmonary Obstruction

Endo Lase, Inc., Washington DC / Traditional, Substantially Equivalent

K844458 is the FDA 510(k) clearance record for ND:YAG LASER PULMONARY OBSTRUCTION, cleared for Endo Lase, Inc. on . FDA records list 24 510(k) clearances for Endo Lase, Inc., from to . As of , FDA records show no recalls naming K844458.

Clearance record

Decision date
Received
(49 days to decision)
Review panel
Unknown
Applicant
Endo Lase, Inc. Attn: Jonathan S. Kahan, Washington DC
Third party review
No