FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SD-200IEHL(TM)
K Number: K914517
·
Decision Jun 30, 1992
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
60
Applicant Total
55
Review Days
265
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Basic Information
- Device Name
- SD-200IEHL(TM)
- K Number
- K914517
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.4480
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Northgate Technologies, Inc.
- Date Received
- October 9, 1991
- Decision Date
- June 30, 1992
- Product Code
- FFK
- 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 |
|---|---|---|---|
| FFK | Lithotriptor, Electro-Hydraulic | FDA class 2 | Gastroenterology, Urology |
Similar 510(k) Clearances
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