FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INTRO-REDUCER (NASOGASTRIC TUBE)
K Number: K875232
·
Decision Jun 2, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
4
Review Days
163
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Basic Information
- Device Name
- INTRO-REDUCER (NASOGASTRIC TUBE)
- K Number
- K875232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Health Improvement Assoc.
- Date Received
- December 22, 1987
- Decision Date
- June 2, 1988
- Product Code
- KNT
- 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 |
|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | FDA class 2 | Gastroenterology, Urology |
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