510(k) K840042
K840042 is an FDA 510(k) premarket notification submitted by Scientific Distributors, Inc. for the device "SDI PREPAX DILUKIT CA". The FDA issued a decision of Substantially Equivalent on February 10, 1984. Scientific Distributors, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 10, 1984
- Date Received
- January 6, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No