Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) 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 the device name listed in this FDA 510(k) record. The listed applicant is Ancora Medical Technology. It received FDA 510(k) clearance on 2020-02-06 under 510(k) 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. The listed applicant is Ancora Medical Technology. The 510(k) number is K191290.

When did Ancora Nerve Block Catheter Set receive FDA 510(k) clearance?

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

Who is the listed applicant for Ancora Nerve Block Catheter Set?

The FDA 510(k) record lists Ancora Medical Technology as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: BSP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.