AMBULASE XAM-15 XANAR SURG. LASER
FDA 510(k) clearance K833325 · decided 1984-01-26
Clearance details
- K-number
- K833325
- Device name
- AMBULASE XAM-15 XANAR SURG. LASER
- Applicant
- Xanar, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1983-09-27
- Decision date
- 1984-01-26
- Days to decision
- 121 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.