510(k) K851875
- Device
- KINNET
- Applicant
- KINETIC CONCEPTS, INC.
- 510(k) number
- K851875
- Product code
- INY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1985-08-22
- Date received
- 1985-04-29
- Regulation
- 890.5180
- Classification name
- Bed, Patient Rotation, Manual
- Medical specialty
- Physical Medicine
- Review panel
- Physical Medicine
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- ROBERT A NEHRMEYER
- Address
- 4958 Stout Dr. San Antonio TX US 78219 78219
FDA Registration Numbers#
- 3014810929
- 3014293077
- 9680168
- 3013846070
- 3010394125
- 3007518294
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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