FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LITHODIAMOND ULTRA
K Number: K061350
·
Decision Dec 22, 2006
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
55
Applicant Total
2
Review Days
221
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Basic Information
- Device Name
- LITHODIAMOND ULTRA
- K Number
- K061350
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5990
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pck Electronic Industry & Trade Co., Ltd.
- Date Received
- May 15, 2006
- Decision Date
- December 22, 2006
- Product Code
- LNS
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| LNS | Lithotriptor, Extracorporeal Shock-Wave, Urological | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Pck Electronic Industry & Trade Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K053279 | UROVANTAGE | Dec 22, 2005 | Substantially Equivalent |