LASER PLUME FILTERS
FDA 510(k) clearance K862954 · decided 1986-08-14
Clearance details
- K-number
- K862954
- Device name
- LASER PLUME FILTERS
- Applicant
- Lifestream Int'L, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-08-05
- Decision date
- 1986-08-14
- Days to decision
- 9 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Sugar Land, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.