510(k) K873478
- Device
- SKYTRON MODEL 130 SURGICAL TABLE
- Applicant
- SKYTRON, DIV. THE KMW GROUP, INC.
- 510(k) number
- K873478
- Product code
- FWY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-09-24
- Date received
- 1987-08-24
- Regulation
- 878.4950
- Classification name
- Table, Operating-room, Non-electrical
- Medical specialty
- General & Plastic Surgery
- Review panel
- General & Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- LARRY J PURCEY
- Address
- 5000 36th St., SE Grand Rapids MI US 49512 49512
FDA Registration Numbers#
- 9680168
- 3004438145
- 3031284260
- 3013875443
- 3008386649
- 1066270
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FWY #
Legacy Summary#
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FDA Review#
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