A1C-CELLULAR
FDA 510(k) clearance K040025 · decided 2004-03-02
Clearance details
- K-number
- K040025
- Device name
- A1C-CELLULAR
- Applicant
- Streck Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2004-01-07
- Decision date
- 2004-03-02
- Days to decision
- 55 days
- Clearance type
- Traditional
- Product code
- JJX
- Device class
- 1
- Regulation number
- 862.1660
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- La Vista, NE, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.