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FDA 510(k)

ESCHMANN DILATION CATHETER

K-Number: K833742 · 1984-04-24

ApplicantVertex Medical Corp.
Decision Date1984-04-24
Product Code
DecisionSubstantially Equivalent

Device Summary

ESCHMANN DILATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vertex Medical Corp.. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K833742. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCHMANN DILATION CATHETER?

ESCHMANN DILATION CATHETER is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Vertex Medical Corp.. The 510(k) number is K833742.

When did ESCHMANN DILATION CATHETER receive FDA 510(k) clearance?

ESCHMANN DILATION CATHETER received FDA 510(k) clearance on 1984-04-24, under 510(k) number K833742.

Who is the listed applicant for ESCHMANN DILATION CATHETER?

The FDA 510(k) record lists Vertex Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Vertex Medical 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.

K834476NEPHROSTOMY/BILIARY DRAINAGE BAGK832380PROTECTIVE SLEEVEK831666SIALOGRAPHY NEEDLEK830576LYMPHANGIOGRAPHY SETK830420POLYETHYLENE MONITORING CONNECTORSK830237TRANSLUCENT POLY. CATH. CONNECTOR AND

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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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