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)

Compact Wearable Pump

K-Number: K230469 · 2023-06-30

Decision Date2023-06-30
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Compact Wearable Pump is a medical device manufactured by Lansinoh Laboratories. It received FDA 510(k) clearance on 2023-06-30 under approval number K230469. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compact Wearable Pump?

Compact Wearable Pump is a medical device that received FDA 510(k) clearance on 2023-06-30. It is manufactured by Lansinoh Laboratories. The 510(k) number is K230469.

When was Compact Wearable Pump approved by the FDA?

Compact Wearable Pump received FDA 510(k) clearance on 2023-06-30, under approval number K230469.

What company makes Compact Wearable Pump?

Compact Wearable Pump is manufactured by Lansinoh Laboratories.

What is the FDA product code for Compact Wearable Pump?

The FDA product code for Compact Wearable Pump is HGX.

Other Devices by Lansinoh Laboratories

Related Devices (Code: HGX)

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.