Atlas FDA

CAL-CHEX CD PLUS

FDA 510(k) clearance K020469 · decided 2002-04-04

Clearance details

K-number
K020469
Device name
CAL-CHEX CD PLUS
Applicant
Streck Laboratories, Inc.
Decision
Substantially Equivalent
Date received
2002-02-12
Decision date
2002-04-04
Days to decision
51 days
Clearance type
Traditional
Product code
KRX
Device class
2
Regulation number
864.8150
Medical specialty
Hematology
Advisory committee
Hematology
Location
La Vista, NE, 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
XN CAL (K160585)Streck2016-12-22
XN CAL (K141962)Streck2014-12-05
XN CAL PF (K141955)Streck2014-12-05
XN CAL PF (K120747)Streck2012-10-22
XN CAL (K120745)Streck2012-10-19
CELL-DYN 22 PLUS CALIBRATOR (K111204)Streck2011-12-22
X-CAL (K083200)Streck2009-02-03
CD-CAL PLUS CALIBRATOR (K003991)R&D Systems, Inc.2001-01-16
CDS LTX CONTROL LATEX PARTICLE SUSPENSION AND PRIMER (K993375)Clinical Diagnostic Solutions, Inc.1999-12-20
CBC-CAL PLUS HEMATOLOGY CALIBRATOR (K955925)R&D Systems, Inc.1996-02-29
3K-CAL HEMATOLOGY CALIBRATOR/MULTIPLE (K912357)R&D Systems, Inc.1991-07-09
CBC-CAL (TM) PLUS/MULTIPLE (K862858)R&D Systems, Inc.1986-08-21

Recalls involving this device

No recalls on record reference this clearance.