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)

FLEX-NECK ARC CATHETER

K-Number: K070730 · 2007-07-03

Decision Date2007-07-03
Product CodeFJS
Advisory CommitteeGU
DecisionUnknown

Device Summary

FLEX-NECK ARC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medigroup, Inc.. It received FDA 510(k) clearance on 2007-07-03 under 510(k) number K070730. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the FLEX-NECK ARC CATHETER?

FLEX-NECK ARC CATHETER is a medical device that received FDA 510(k) clearance on 2007-07-03. The listed applicant is Medigroup, Inc.. The 510(k) number is K070730.

When did FLEX-NECK ARC CATHETER receive FDA 510(k) clearance?

FLEX-NECK ARC CATHETER received FDA 510(k) clearance on 2007-07-03, under 510(k) number K070730.

Who is the listed applicant for FLEX-NECK ARC CATHETER?

The FDA 510(k) record lists Medigroup, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEX-NECK ARC CATHETER?

The FDA product code for FLEX-NECK ARC CATHETER is FJS.

Related Clinical Trials

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.

Other records listing Medigroup, Inc. as applicant

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.

Related Devices (Code: FJS)

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.

↑