SDI PREPAX DILUKIT CA
FDA 510(k) clearance K840042 · decided 1984-02-10
Clearance details
- K-number
- K840042
- Device name
- SDI PREPAX DILUKIT CA
- Applicant
- Scientific Distributors, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-01-06
- Decision date
- 1984-02-10
- Days to decision
- 35 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- 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.