K840042Substantially Equivalent
Sdi Prepax Dilukit Ca
Scientific Distributors, Inc., Mchenry IL / Traditional, Substantially Equivalent
K840042 is the FDA 510(k) clearance record for SDI PREPAX DILUKIT CA, cleared for Scientific Distributors, Inc. on . FDA records list 7 510(k) clearances for Scientific Distributors, Inc., from to . As of , FDA records show no recalls naming K840042.
Clearance record
- Decision date
- Received
- (35 days to decision)
- Review panel
- Unknown
- Applicant
- Scientific Distributors, Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
