FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RIGHT ANGLE UROLOGIC LASER FIBER
K Number: K943491
·
Decision Aug 5, 1994
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
29
Review Days
17
Basic Information
- Device Name
- RIGHT ANGLE UROLOGIC LASER FIBER
- K Number
- K943491
- 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
- SURGITEK
- Date Received
- July 19, 1994
- Decision Date
- August 5, 1994
- 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 SURGITEK
| K Number | Device Name | ||
|---|---|---|---|
| K946296 | QUADRA-COIL URETERAL STENT | Mar 6, 1995 | Substantially Equivalent |
| K944391 | OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM | Feb 7, 1995 | Substantially Equivalent |
| K941952 | SURGITEK INFUSER | May 24, 1994 | Substantially Equivalent |
| K933260 | HELICAL STONE/FLATWIRE STONE BASKETS | Jan 11, 1994 | Substantially Equivalent |
| K933261 | GRASPING FORCEPS | Jan 11, 1994 | Substantially Equivalent |
| K930733 | URETERAL STENT | Jul 23, 1993 | Substantially Equivalent |
| K930483 | URETERAL CATHETER | Jul 16, 1993 | Unknown |
| K926344 | HYDROPHILIC COATED GUIDEWIRE | Mar 5, 1993 | Substantially Equivalent |
| K920451 | ENDOTEK ULTRA SYSTEM | Sep 17, 1992 | Substantially Equivalent |
| K922542 | GRASPING FORCEPS | Aug 19, 1992 | Substantially Equivalent |