IL TEST(TM) PRO-CHROM
FDA 510(k) clearance K924884 · decided 1993-01-14
Clearance details
- K-number
- K924884
- Device name
- IL TEST(TM) PRO-CHROM
- Applicant
- Instrumentation Laboratory CO
- Decision
- Substantially Equivalent
- Date received
- 1992-09-28
- Decision date
- 1993-01-14
- Days to decision
- 108 days
- Clearance type
- Traditional
- Product code
- GGP
- Device class
- 2
- Regulation number
- 864.7290
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Lexington, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.