FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PRENVAL I
K Number: K953652
·
Decision Sep 15, 1995
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
77
Applicant Total
3
Review Days
39
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Basic Information
- Device Name
- PRENVAL I
- K Number
- K953652
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2100
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Base Ten Systems, Inc.
- Date Received
- August 7, 1995
- Decision Date
- September 15, 1995
- Product Code
- JQP
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| JQP | Calculator/Data Processing Module, For Clinical Use | FDA class 1 | Clinical Chemistry |
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