MICROSCOPE STAGE HEATER
FDA 510(k) clearance K881467 · decided 1988-04-18
Clearance details
- K-number
- K881467
- Device name
- MICROSCOPE STAGE HEATER
- Applicant
- Cryodyne Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-06
- Decision date
- 1988-04-18
- Days to decision
- 12 days
- Clearance type
- Traditional
- Product code
- KEJ
- Device class
- 1
- Regulation number
- 864.3600
- Medical specialty
- Pathology
- Advisory committee
- Pathology
- 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.