LIBERTY HOT PACK AND LIBERTY KOLD PACK
FDA 510(k) clearance K902839 · decided 1990-07-25
Clearance details
- K-number
- K902839
- Device name
- LIBERTY HOT PACK AND LIBERTY KOLD PACK
- Applicant
- Liberty Ent.
- Decision
- Substantially Equivalent
- Date received
- 1990-06-28
- Decision date
- 1990-07-25
- Days to decision
- 27 days
- Clearance type
- Traditional
- Product code
- IMD
- Device class
- 1
- Regulation number
- 890.5710
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Amsterdam, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.