FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PRIMUS HOLLOW FIBER DIALYZER MOD. 1000, 1350, 2000
K Number: K923727
·
Decision Jul 29, 1994
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
336
Applicant Total
33
Review Days
732
Basic Information
- Device Name
- PRIMUS HOLLOW FIBER DIALYZER MOD. 1000, 1350, 2000
- K Number
- K923727
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5860
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MINNTECH CORP.
- Date Received
- July 27, 1992
- Decision Date
- July 29, 1994
- Product Code
- KDI
- 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 |
|---|---|---|---|
| KDI | Dialyzer, High Permeability With Or Without Sealed Dialysate System | FDA class 2 | Gastroenterology, Urology |
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FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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