510(k) K780890
- Device
- CAPP TERMINAL DEVICE
- Applicant
- HOSMER DORRANCE CORP.
- 510(k) number
- K780890
- Product code
- IQX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-06-13
- Date received
- 1978-05-31
- Regulation
- 890.3420
- Classification name
- Hook, External Limb Component, Mechanical
- Medical specialty
- Physical Medicine
- Review panel
- Physical Medicine
- 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#
- 2950684
- 9616494
- 1022826
- 9617046
- 3007914557
- 3039489396
- 3012881757
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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