CRYOBIOLOGICAL FREEZER
FDA 510(k) clearance K881465 · decided 1988-04-21
Clearance details
- K-number
- K881465
- Device name
- CRYOBIOLOGICAL FREEZER
- Applicant
- Cryodyne Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-06
- Decision date
- 1988-04-21
- Days to decision
- 15 days
- Clearance type
- Traditional
- Product code
- KSP
- Device class
- 1
- Regulation number
- 864.9225
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Soquel, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.