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)

babyLance Safety Heelstick (BLM, BLN, BLP)

K-Number: K223900 · 2023-02-24

Decision Date2023-02-24
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

babyLance Safety Heelstick (BLM, BLN, BLP) is a medical device manufactured by Clinical Innovations, LLC. It received FDA 510(k) clearance on 2023-02-24 under approval number K223900. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the babyLance Safety Heelstick (BLM, BLN, BLP)?

babyLance Safety Heelstick (BLM, BLN, BLP) is a medical device that received FDA 510(k) clearance on 2023-02-24. It is manufactured by Clinical Innovations, LLC. The 510(k) number is K223900.

When was babyLance Safety Heelstick (BLM, BLN, BLP) approved by the FDA?

babyLance Safety Heelstick (BLM, BLN, BLP) received FDA 510(k) clearance on 2023-02-24, under approval number K223900.

What company makes babyLance Safety Heelstick (BLM, BLN, BLP)?

babyLance Safety Heelstick (BLM, BLN, BLP) is manufactured by Clinical Innovations, LLC.

What is the FDA product code for babyLance Safety Heelstick (BLM, BLN, BLP)?

The FDA product code for babyLance Safety Heelstick (BLM, BLN, BLP) is FMK.

Other Devices by Clinical Innovations, LLC

Related Devices (Code: FMK)

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.