Atlas FDA

COULTER MEAN PLATELET VOLUME CALIBRATOR

FDA 510(k) clearance K843910 · decided 1985-01-07

Clearance details

K-number
K843910
Device name
COULTER MEAN PLATELET VOLUME CALIBRATOR
Applicant
Coulter Electronics, Inc.
Decision
Substantially Equivalent
Date received
1984-10-03
Decision date
1985-01-07
Days to decision
96 days
Clearance type
Traditional
Product code
KRY
Device class
2
Regulation number
864.8175
Medical specialty
Hematology
Advisory committee
Hematology
Location
Hialeah, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
S-CAL HEMATOLOGY CALIBRATOR (K862122)Coulter Electronics, Inc.1987-05-20
LASER PLATELETCAL/MULTIPLE (K852016)R&D Systems, Inc.1985-07-09
S-CAL HEMATOLOGY CALIBRATOR (K840794)Coulter Electronics, Inc.1984-04-04
CONTROL DIAGNOSTICS PLATELET CONTROL (K821851)Immunogenetics1982-09-02
TEKNI-CAL (K781601)Streck Laboratories, Inc.1978-10-10
PC-CALIBRATOR (K781133)Streck Laboratories, Inc.1978-08-14
TQC CALIBRATION REFERENCE FOR PLATELETS (K770143)Technicon Instruments Corp.1978-01-30

Recalls involving this device

No recalls on record reference this clearance.