FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHT
K Number: K133425
·
Decision Dec 5, 2013
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
28
Applicant Total
2
Review Days
27
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Basic Information
- Device Name
- SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHT
- K Number
- K133425
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.4580
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Engineered Medical Solutions Co., LLC
- Date Received
- November 8, 2013
- Decision Date
- December 5, 2013
- Product Code
- FTD
- 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 |
|---|---|---|---|
| FTD | Lamp, Surgical | FDA class 2 | General, Plastic Surgery |
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SCINTILLANT SURGICAL LIGHT, MODEL 2644-01-0001
FDA 510(k)
FDA Class 2
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Other Clearances by Engineered Medical Solutions Co., LLC
| K Number | Device Name | ||
|---|---|---|---|
| K071180 | SCINTILLANT SURGICAL LIGHT, MODEL 2644-01-0001 | Jun 20, 2007 | Substantially Equivalent |