ND:YAG LASER PULMONARY OBSTRUCTION
FDA 510(k) clearance K844458 · decided 1985-01-03
Clearance details
- K-number
- K844458
- Device name
- ND:YAG LASER PULMONARY OBSTRUCTION
- Applicant
- Endo Lase, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-11-15
- Decision date
- 1985-01-03
- Days to decision
- 49 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.