KINNET
FDA 510(k) clearance K851875 · decided 1985-08-22
Clearance details
- K-number
- K851875
- Device name
- KINNET
- Applicant
- Kinetic Concepts, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1985-04-29
- Decision date
- 1985-08-22
- Days to decision
- 115 days
- Clearance type
- Traditional
- Product code
- INY
- Device class
- 1
- Regulation number
- 890.5180
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- San Antonio, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.