Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Mckinley, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K042228	BEELINE MOTIV, PROPOLIS, PCA	FRN	2004-11-08	View
510(k)	K033039	MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS	MEB	2003-10-07	View
510(k)	K032642	BEELINE SYSTEM	FRN	2003-09-23	View
510(k)	K991275	WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS	FRN	1999-07-01	View
510(k)	K990461	MCKINLEY SP DISPOSABLE INFUSION PUMP	MEB	1999-06-30	View
510(k)	K982256	OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMP	MEB	1998-09-30	View
510(k)	K971844	MCKINLEY OUTBOUND-2 SYSTEM	FPA	1998-01-23	View

↑