FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TSX PROBE, OCULAR CONTACT PROBE;TSX PROBE,OCULAR CONTACT PROBE,SMA
K Number: K992508
·
Decision Aug 19, 1999
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
2
Review Days
23
Basic Information
- Device Name
- TSX PROBE, OCULAR CONTACT PROBE;TSX PROBE,OCULAR CONTACT PROBE,SMA
- K Number
- K992508
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- INSTRUMENTS FOR MEDICINE AND DIAGNOSTICS
- Date Received
- July 27, 1999
- Decision Date
- August 19, 1999
- 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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Other Clearances by INSTRUMENTS FOR MEDICINE AND DIAGNOSTICS
| K Number | Device Name | ||
|---|---|---|---|
| K981952 | COMBINATION ND:YAG AND FREQUENCY DOUBLED SOLID STATE GREEN LASER | Sep 1, 1998 | Substantially Equivalent |