Atlas FDA

LYPHOCHECK URINE METALS CONTROL, ITEM NO.400, 405

FDA 510(k) clearance K990928 · decided 1999-04-16

Clearance details

K-number
K990928
Device name
LYPHOCHECK URINE METALS CONTROL, ITEM NO.400, 405
Applicant
Bio-Rad
Decision
Substantially Equivalent
Date received
1999-03-19
Decision date
1999-04-16
Days to decision
28 days
Clearance type
Traditional
Product code
DIE
Device class
1
Regulation number
862.3280
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Irvine, CA, 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
LYPHOCHEK WHOLE BLOOD METALS CONTROL MODEL # 527, 528, 529 (K020610)Bio-Rad2002-04-22
LYPHOCHEK URINE METALS CONTROL, LEVELS I AND II (K891691)Bio-Rad1989-12-19
SHAPE-ACTIO METAL TOXICOLOGY CONTROL (K890721)Actio, Inc.1989-04-10
SHAPE-ACTIO METAL TOXICOLOGY CONTROL (K863915)Shape Products Co.1986-11-24

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S002)Bio-Rad1996-03-01
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S001)Bio-Rad1991-03-14
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032)Bio-Rad1989-07-24