AUTO-TENS MODEL I DISPOS. SINGLE CHAN
FDA 510(k) clearance K823467 · decided 1983-02-07
Clearance details
- K-number
- K823467
- Device name
- AUTO-TENS MODEL I DISPOS. SINGLE CHAN
- Applicant
- Cbc Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-11-19
- Decision date
- 1983-02-07
- Days to decision
- 80 days
- Clearance type
- Traditional
- Product code
- GZJ
- Device class
- 2
- Regulation number
- 882.5890
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.