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Company · US

Western Laboratories Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1984. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FIZ	Meter, Conductivity, Non-Remote	1
FKQ	System, Dialysate Delivery, Central Multiple Patient	1
FLB	Meter, Conductivity, Induction, Remote Type	1
FTZ	Locator, Magnetic	1
KDI	Dialyzer, High Permeability With Or Without Sealed Dialysate System	1
KFF	Assay, Heparin	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jun 11, 1984	K834024	HEPARINOMETER Western Laboratories Corp.	KFF
Apr 12, 1983	K830468	MODEL 200 Western Laboratories Corp.	FTZ
Jul 2, 1982	K821834	MODEL 100 BICARBONATE CONDUCTIVITY Western Laboratories Corp.	FKQ
May 27, 1982	K821415	MODEL 90 BC Western Laboratories Corp.	FLB
May 27, 1982	K821414	MODEL 80 BC Western Laboratories Corp.
Jul 28, 1980	K801303	MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TEST Western Laboratories Corp.	KDI
Aug 31, 1978	K780932	MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT Western Laboratories Corp.	FIZ

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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