FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Delta III Lithotripter
K Number: K172084
·
Decision Aug 8, 2017
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
55
Applicant Total
40
Review Days
29
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Basic Information
- Device Name
- Delta III Lithotripter
- K Number
- K172084
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 876.5990
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dornier Medtech America, Inc.
- Date Received
- July 10, 2017
- Decision Date
- August 8, 2017
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LNS), ordered by most recent decision date.
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