Beeline Motiv, Propolis, PCA
510(k) K042228
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK042228 | Date8 Nov 2004 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- FRN
- Device Class
- Class II
- Regulation
- 21 CFR Part 880.5725
- Advisory Committee
- General Hospital
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 25 Sep 2026
The Beeline Motiv, Propolis, PCA is a Class II infusion pump manufactured by McKinley, Inc. It is designed for use in general hospital settings to deliver controlled amounts of medication or fluids to patients.
This device is supplied as a single-use or reusable product, though specific sterility information is not provided in the data. It has received FDA 510(k) clearance with the number K042228 and is classified under regulation number 880.5725. The device is available in various models as indicated by the multiple registration numbers associated with it.
Other devices from Mckinley, Inc.
Questions
AI-generated answers, 25 Sep 2026
What is the Beeline Motiv infusion pump used for?
The Beeline Motiv infusion pump is designed to deliver controlled amounts of medication or fluids to patients in general hospital settings.
Is the Beeline Motiv infusion pump single-use or reusable?
The Beeline Motiv infusion pump is supplied as either a single-use or reusable product, though specific sterility information is not provided.
What regulatory clearance has the Beeline Motiv infusion pump received?
The Beeline Motiv infusion pump has received FDA 510(k) clearance with the number K042228.