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)

DEKA ACE Pump System

K-Number: K241178 · 2024-05-24

Decision Date2024-05-24
Product CodeQFG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DEKA ACE Pump System is a medical device manufactured by Deka Research and Development. It received FDA 510(k) clearance on 2024-05-24 under approval number K241178. The device is classified under product code QFG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKA ACE Pump System?

DEKA ACE Pump System is a medical device that received FDA 510(k) clearance on 2024-05-24. It is manufactured by Deka Research and Development. The 510(k) number is K241178.

When was DEKA ACE Pump System approved by the FDA?

DEKA ACE Pump System received FDA 510(k) clearance on 2024-05-24, under approval number K241178.

What company makes DEKA ACE Pump System?

DEKA ACE Pump System is manufactured by Deka Research and Development.

What is the FDA product code for DEKA ACE Pump System?

The FDA product code for DEKA ACE Pump System is QFG.

Other Devices by Deka Research and Development

View all 10 devices →

Related Devices (Code: QFG)

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.