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FDA 510(k)

TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME

K-Number: K850764 · 1985-05-10

ApplicantAston & Aston
Decision Date1985-05-10
Product Code
DecisionSubstantially Equivalent

Device Summary

TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME is the device name listed in this FDA 510(k) record. The listed applicant is Aston & Aston. It received FDA 510(k) clearance on 1985-05-10 under 510(k) number K850764. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME?

TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME is a medical device that received FDA 510(k) clearance on 1985-05-10. The listed applicant is Aston & Aston. The 510(k) number is K850764.

When did TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME receive FDA 510(k) clearance?

TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME received FDA 510(k) clearance on 1985-05-10, under 510(k) number K850764.

Who is the listed applicant for TAUCHER TUNNELER-PERIPHERAL VASCULAR SURG-INSTRUME?

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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