510(k) K896092
- Device
- ALKALINE PHOSPHATASE, LEUKOCYTE, KIT
- Applicant
- SIGMA CHEMICAL CO.
- 510(k) number
- K896092
- Product code
- GHD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1989-11-09
- Date received
- 1989-10-19
- Regulation
- 864.7660
- Classification name
- Test, Leukocyte Alkaline Phosphatase
- Medical specialty
- Hematology
- Review panel
- Hematology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- TAKES, PHD
- Address
- 545 S. Ewing Ave. St. Louis MO US 63103 63103
FDA Registration Numbers#
- 1836161
- 8030607
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code GHD #
Legacy Summary#
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FDA Review#
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