PROACTIVATOR C3, C4 AND C3
FDA 510(k) clearance K790059 · decided 1979-03-15
Clearance details
- K-number
- K790059
- Device name
- PROACTIVATOR C3, C4 AND C3
- Applicant
- Icl Scientific
- Decision
- Substantially Equivalent
- Date received
- 1979-01-09
- Decision date
- 1979-03-15
- Days to decision
- 65 days
- Clearance type
- Traditional
- Product code
- KTP
- Device class
- 2
- Regulation number
- 866.5260
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.