LIMB-GUARD
FDA 510(k) clearance K863964 · decided 1986-10-24
Clearance details
- K-number
- K863964
- Device name
- LIMB-GUARD
- Applicant
- Sparco, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-10-10
- Decision date
- 1986-10-24
- Days to decision
- 14 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Castro Valley, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.