DYNATRON 900
FDA 510(k) clearance K993919 · decided 2000-01-03
Clearance details
- K-number
- K993919
- Device name
- DYNATRON 900
- Applicant
- Dynatronics Corp.
- Decision
- Substantially Equivalent
- Date received
- 1999-11-18
- Decision date
- 2000-01-03
- Days to decision
- 46 days
- Clearance type
- Traditional
- Product code
- ITH
- Device class
- 2
- Regulation number
- 890.5900
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Salt Lake City, UT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.