FDA 510(k)
Substantially Equivalent
🇺🇸 United States
SDI PREPAX DILUKIT CA
K Number: K840042
·
Decision Feb 10, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
7
Review Days
35
Basic Information
- Device Name
- SDI PREPAX DILUKIT CA
- K Number
- K840042
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- SCIENTIFIC DISTRIBUTORS, INC.
- Date Received
- January 6, 1984
- Decision Date
- February 10, 1984
- Advisory Committee
- Unknown
- Review Advisory Committee
- HE
- Third Party
- N
Other Clearances by SCIENTIFIC DISTRIBUTORS, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K892658 | SDI PREPAX COUNTAPETTE KIT | May 24, 1989 | Substantially Equivalent |
| K851320 | SDI PREPAX DILUKIT M. | Jul 5, 1985 | Substantially Equivalent |
| K840044 | SDI PREPAX DILUKIT 29-1000 | Mar 9, 1984 | Substantially Equivalent |
| K840041 | SDI PREPAX DILUKIT HW | Mar 5, 1984 | Substantially Equivalent |
| K840043 | SDI PREPAX DILUKIT CT | Feb 10, 1984 | Substantially Equivalent |
| K840038 | PREPAX DILUKIT PLUS | Feb 10, 1984 | Substantially Equivalent |