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FDA 510(k)

YASARGIL SUCTION TUBE - LARGE

K-Number: K760746 · 1976-11-01

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-01
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YASARGIL SUCTION TUBE - LARGE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760746. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YASARGIL SUCTION TUBE - LARGE?

YASARGIL SUCTION TUBE - LARGE is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K760746.

When did YASARGIL SUCTION TUBE - LARGE receive FDA 510(k) clearance?

YASARGIL SUCTION TUBE - LARGE received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760746.

Who is the listed applicant for YASARGIL SUCTION TUBE - LARGE?

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

What is the FDA product code for YASARGIL SUCTION TUBE - LARGE?

The FDA product code for YASARGIL SUCTION TUBE - LARGE is GCY.

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Related Devices (Code: GCY)

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.

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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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