FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DYE CURVE EVALUATOR
K Number: K792135
·
Decision Jan 11, 1980
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
1
Review Days
81
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Basic Information
- Device Name
- DYE CURVE EVALUATOR
- K Number
- K792135
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1425
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Sci-Pro, Inc.
- Date Received
- October 22, 1979
- Decision Date
- January 11, 1980
- Product Code
- DQK
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQK | Computer, Diagnostic, Programmable | FDA class 2 | Cardiovascular |
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