SHARPLAN LASER POSITIONING SYSTEM
FDA 510(k) clearance K837573 · decided 1983-06-28
Clearance details
- K-number
- K837573
- Device name
- SHARPLAN LASER POSITIONING SYSTEM
- Applicant
- Laser Industries , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1983-05-27
- Decision date
- 1983-06-28
- Days to decision
- 32 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Tel Aviv, IL
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.