CURAMED 402
FDA 510(k) clearance K850573 · decided 1985-05-17
Clearance details
- K-number
- K850573
- Device name
- CURAMED 402
- Applicant
- Fluidotherapy Corp.
- Decision
- Substantially Equivalent
- Date received
- 1985-02-13
- Decision date
- 1985-05-17
- Days to decision
- 93 days
- Clearance type
- Traditional
- Product code
- IMJ
- Device class
- 2
- Regulation number
- 890.5290
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Houston, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.