CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A— 510(k) K032951
Substantially EquivalentChrono-Log Corp.
FDA 510(k) clearance K032951 for CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A, Substantially Equivalent on 2004-04-02. Applicant: Chrono-Log Corp.. Device class: 2.
Clearance details
- Applicant
- Chrono-Log Corp.
- Product code
- Code JOZ
- Device class
- Class 2
- Regulation
- 21 CFR 864.5700
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Havertown, PA, US
Recent devices under product code JOZ
view all- K191364 — T-TAS 01 Total Thrombus-formation Analysis System Instrument, PL Chip for T-TAS 01, PL Chip Reservoir Set for T-TAS 01, BAPA tube for T-TAS 01
- K181777 — AggreGuide A-100 ADP
- K163274 — AggreGuide A-100 AA Assay, AggreGuide A-100 Instrument
- K161329 — Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channel
- K141427 — ACCUMETRICS,INC. VERIFYNOW PRUTEST, ACCUMETRICS, INC. VERIFYNOW PRUTEST
More clearances from Chrono-Log Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.