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)

IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK

K-Number: K954622 · 1996-04-29

Decision Date1996-04-29
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific /International Technologies. It received FDA 510(k) clearance on 1996-04-29 under 510(k) number K954622. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK?

IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK is a medical device that received FDA 510(k) clearance on 1996-04-29. The listed applicant is Boston Scientific /International Technologies. The 510(k) number is K954622.

When did IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK receive FDA 510(k) clearance?

IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK received FDA 510(k) clearance on 1996-04-29, under 510(k) number K954622.

Who is the listed applicant for IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK?

The FDA 510(k) record lists Boston Scientific /International Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK?

The FDA product code for IVT 0.014 TRACK OR IVT 0.014 ACCUTRACK is DQX.

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 Boston Scientific /International Technologies 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: DQX)

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.

↑