FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYST
K Number: K924647
·
Decision Jun 4, 1993
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
5
Review Days
263
Basic Information
- Device Name
- DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYST
- K Number
- K924647
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- DERMA-LASE CO.
- Date Received
- September 14, 1992
- Decision Date
- June 4, 1993
- Product Code
- GEX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | FDA class 2 | General, Plastic Surgery |
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