SHARPLAN 721 CO2 SURGICAL LASER
FDA 510(k) clearance K837342 · decided 1983-05-18
Clearance details
- K-number
- K837342
- Device name
- SHARPLAN 721 CO2 SURGICAL LASER
- Applicant
- Laser Industries , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1983-03-08
- Decision date
- 1983-05-18
- Days to decision
- 71 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Tel Aviv, IL
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Laser Industries
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Recalls involving this device
No recalls on record reference this clearance.