MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
FDA 510(k) clearance K827506 · decided 1982-06-11
Clearance details
- K-number
- K827506
- Device name
- MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
- Applicant
- Merrimack Laboratories
- Decision
- Substantially Equivalent
- Date received
- 1982-05-04
- Decision date
- 1982-06-11
- Days to decision
- 38 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Hudson, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.