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)

Ancora Nerve Block Catheter Set

K-Number: K191290 · 2020-02-06

Decision Date2020-02-06
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Ancora Nerve Block Catheter Set is a medical device manufactured by Ancora Medical Technology. It received FDA 510(k) clearance on 2020-02-06 under approval number K191290. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ancora Nerve Block Catheter Set?

Ancora Nerve Block Catheter Set is a medical device that received FDA 510(k) clearance on 2020-02-06. It is manufactured by Ancora Medical Technology. The 510(k) number is K191290.

When was Ancora Nerve Block Catheter Set approved by the FDA?

Ancora Nerve Block Catheter Set received FDA 510(k) clearance on 2020-02-06, under approval number K191290.

What company makes Ancora Nerve Block Catheter Set?

Ancora Nerve Block Catheter Set is manufactured by Ancora Medical Technology.

What is the FDA product code for Ancora Nerve Block Catheter Set?

The FDA product code for Ancora Nerve Block Catheter Set is BSP.

Related Clinical Trials

Related Devices (Code: BSP)

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.