THERMO-PACK
FDA 510(k) clearance K890924 · decided 1989-03-14
Clearance details
- K-number
- K890924
- Device name
- THERMO-PACK
- Applicant
- Medical Manufacturers, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-02-24
- Decision date
- 1989-03-14
- Days to decision
- 18 days
- Clearance type
- Traditional
- Product code
- IMD
- Device class
- 1
- Regulation number
- 890.5710
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Englewood, CO, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.