DYNA-LYTE 2000
FDA 510(k) clearance K842786 · decided 1984-09-14
Clearance details
- K-number
- K842786
- Device name
- DYNA-LYTE 2000
- Applicant
- Abbott Diagnostics
- Decision
- Substantially Equivalent
- Date received
- 1984-05-22
- Decision date
- 1984-09-14
- Days to decision
- 115 days
- Clearance type
- Traditional
- Product code
- CEM
- Device class
- 2
- Regulation number
- 862.1600
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Mountain View, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.