CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH
K-Number: K924980 · 1993-01-15
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Device Summary
Frequently Asked Questions
What is the CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH?
CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Endosonics Corp.. The 510(k) number is K924980.
When did CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH receive FDA 510(k) clearance?
CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH received FDA 510(k) clearance on 1993-01-15, under 510(k) number K924980.
Who is the listed applicant for CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH?
The FDA 510(k) record lists Endosonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH?
The FDA product code for CATHSCANNER VISIONS MICRORAIL ULTRA IMAG CATH is ITX.
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 Endosonics Corp. 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: ITX)
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.
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