FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
GI BLEEDER/OD SET
K Number: K913476
·
Decision Feb 12, 1992
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
66
Review Days
191
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Basic Information
- Device Name
- GI BLEEDER/OD SET
- K Number
- K913476
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Unknown
- Statement or Summary
- Statement
- Applicant
- Icu Medical, Inc.
- Date Received
- August 5, 1991
- Decision Date
- February 12, 1992
- 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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