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
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