KIN-COM JR
FDA 510(k) clearance K881388 · decided 1988-04-21
Clearance details
- K-number
- K881388
- Device name
- KIN-COM JR
- Applicant
- Chattanooga Group, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-04
- Decision date
- 1988-04-21
- Days to decision
- 17 days
- Clearance type
- Traditional
- Product code
- LBB
- Device class
- 2
- Regulation number
- 888.1240
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Red Bank, TN, US
- Third-party review
- No
- Expedited review
- No
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| DYNAMOMETER (K964685) | John Chatillon & Sons, Inc. | 1997-01-27 |
| GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM (K935757) | Greenleaf Medical Systems, Inc. | 1994-04-15 |
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| NK GRASP SENSOR, MODEL GA002 (K923965) | Nk Biotechnical Engineering Co. | 1993-05-12 |
Recalls involving this device
No recalls on record reference this clearance.