510(k) K781516
- Device
- TEST SYSTEM TISSUE CELL CULTURE SLIDE
- Applicant
- ZEUS SCIENTIFIC, INC.
- 510(k) number
- K781516
- Product code
- KIY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-09-27
- Date received
- 1978-08-31
- Regulation
- 864.2240
- Classification name
- Chamber, Slide Culture
- Medical specialty
- Hematology
- Review panel
- Pathology
- 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
- 3006788232
- 3010420046
- 1423662
- 3006673317
- 3045058049
- 2242436
- 3015505238
- 2029372
- 1219230
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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