510(k) K831079
- Device
- Liquipette
- Applicant
- THE KENDALL COMPANY DIV. OF TYCO HEALTHCARE GROUP
- 510(k) number
- K831079
- Product code
- GJG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1983-04-28
- Date received
- 1983-04-04
- Regulation
- 864.6160
- Classification name
- Pipette, Quantitative, Hematology
- Medical specialty
- Hematology
- Review panel
- Hematology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3010131137
- 2916657
- 3010194621
- 2244900
- 1618982
Source Documents#
510(k) summary PDF not indicated by FDA