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)

OCHSNER ULP BIFURCATION VASCULAR PROTHESIS

K-Number: K913143 · 1991-10-23

Decision Date1991-10-23
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OCHSNER ULP BIFURCATION VASCULAR PROTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Intervascular, Inc.. It received FDA 510(k) clearance on 1991-10-23 under 510(k) number K913143. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCHSNER ULP BIFURCATION VASCULAR PROTHESIS?

OCHSNER ULP BIFURCATION VASCULAR PROTHESIS is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Intervascular, Inc.. The 510(k) number is K913143.

When did OCHSNER ULP BIFURCATION VASCULAR PROTHESIS receive FDA 510(k) clearance?

OCHSNER ULP BIFURCATION VASCULAR PROTHESIS received FDA 510(k) clearance on 1991-10-23, under 510(k) number K913143.

Who is the listed applicant for OCHSNER ULP BIFURCATION VASCULAR PROTHESIS?

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

What is the FDA product code for OCHSNER ULP BIFURCATION VASCULAR PROTHESIS?

The FDA product code for OCHSNER ULP BIFURCATION VASCULAR PROTHESIS is DSY.

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 Intervascular, 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.

View all 16 devices →

Related Devices (Code: DSY)

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.

↑