MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS
FDA 510(k) clearance K932240 · decided 1994-04-01
Clearance details
- K-number
- K932240
- Device name
- MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS
- Applicant
- Bailey Mfg. Co.
- Decision
- Substantially Equivalent
- Date received
- 1993-05-07
- Decision date
- 1994-04-01
- Days to decision
- 329 days
- Clearance type
- Traditional
- Product code
- IRR
- Device class
- 1
- Regulation number
- 890.5380
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Lodi, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.