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)

ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR

K-Number: K062241 · 2006-11-09

Decision Date2006-11-09
Product CodeJAQ
Advisory CommitteeRA
DecisionUnknown

Device Summary

ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR is the device name listed in this FDA 510(k) record. The listed applicant is North American Scientific, Inc.. It received FDA 510(k) clearance on 2006-11-09 under 510(k) number K062241. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR?

ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR is a medical device that received FDA 510(k) clearance on 2006-11-09. The listed applicant is North American Scientific, Inc.. The 510(k) number is K062241.

When did ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR receive FDA 510(k) clearance?

ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR received FDA 510(k) clearance on 2006-11-09, under 510(k) number K062241.

Who is the listed applicant for ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR?

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

What is the FDA product code for ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR?

The FDA product code for ADJUSTABLE MULTI-CATHETER SOURCE APPLICTOR is JAQ.

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 North American Scientific, 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: JAQ)

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.

↑