ECLIPSE ICA BUN
FDA 510(k) clearance K905602 · decided 1991-01-16
Clearance details
- K-number
- K905602
- Device name
- ECLIPSE ICA BUN
- Applicant
- Biotope, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-12-13
- Decision date
- 1991-01-16
- Days to decision
- 34 days
- Clearance type
- Traditional
- Product code
- CDQ
- Device class
- 2
- Regulation number
- 862.1770
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Redmond, WA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.