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

FDA 510(k)

Solution Administration Sets

K-Number: K243529 · 2025-03-14

Decision Date2025-03-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Solution Administration Sets is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2025-03-14 under approval number K243529. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Solution Administration Sets?

Solution Administration Sets is a medical device that received FDA 510(k) clearance on 2025-03-14. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K243529.

When was Solution Administration Sets approved by the FDA?

Solution Administration Sets received FDA 510(k) clearance on 2025-03-14, under approval number K243529.

What company makes Solution Administration Sets?

Solution Administration Sets is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for Solution Administration Sets?

The FDA product code for Solution Administration Sets is FPA.

Related Clinical Trials

Other Devices by Baxter Healthcare Corporation

View all 48 devices →

Related Devices (Code: FPA)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.