FDA Device Entity Profile: CLINIQA CORPORATION

Known Identifiers & Locations

FEI Numbers 1000135102, 3010725882

Owner Operator Numbers 2083131

Locations Covered San Marcos, CA, US

Registered Establishments (2)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2085064	CLINIQA CORPORATION	San Marcos, CA, US	Manufacture Medical Device	View Details
3010725882	CLINIQA CORPORATION	San Marcos, CA, US	Manufacture Medical Device	View Details

510(k) Premarket Notifications (1)

Submission #	Device Name	Decision Date	Decision Description	Action
K060322	CLINIQA DRY QC CHEMISTRY CONTROL, LEVELS 1 AND 2, ASSAYED, CLINIQA DRY QC CHEMISTRY CONTROL, LEVEL 1 AND 2 UNASSAYED	2006-03-21	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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