510(k) K810899
- Device
- Technicon Autogrouper 16-c System
- Applicant
- TECHNICON INSTRUMENTS CORP.
- 510(k) number
- K810899
- Product code
- KSZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1981-05-05
- Date received
- 1981-04-03
- Regulation
- 864.9175
- Classification name
- System, Test, Automated Blood Grouping And Antibody
- Medical specialty
- Hematology
- Review panel
- Hematology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3003783142
- 2032600
- 9610824
- 3006198300
- 1531264
- 9612296
- 1217454
- 3003402518
- 3012963943
- 3003966680
- 2250051
- 3004910133
- 3021186226
- 1643621
- 1034569
- 3016014873
- 3002642396
- 3006421415
- 3008244372
- 3000236920
- 3002772505
- 1319681
- 3013557562
- 3020460367
- 8043379
- 3000308930
- 1056600
- 3014643041
Source Documents#
510(k) summary PDF not indicated by FDA