Mckinley, Inc.
Mckinley, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2004.
Top product codes for Mckinley, Inc.
Recent clearances by Mckinley, Inc.
- K042228 — BEELINE MOTIV, PROPOLIS, PCA
- K033039 — MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS
- K032642 — BEELINE SYSTEM
- K991275 — WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS
- K990461 — MCKINLEY SP DISPOSABLE INFUSION PUMP
- K982256 — OUTBOUND DISPOSABLE SYRINGE INFUSER OUTBOUND 2 DISPOSABLE PUMP
- K971844 — MCKINLEY OUTBOUND-2 SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.