FDA 510(k)

SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER

K-Number: K914009 · 1991-12-06

Decision Date1991-12-06

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Schneider Intl., Ltd.. It received FDA 510(k) clearance on 1991-12-06 under 510(k) number K914009. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER?

SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1991-12-06. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K914009.

When did SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1991-12-06, under 510(k) number K914009.

Who is the listed applicant for SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER?

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

What is the FDA product code for SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER?

The FDA product code for SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER is DQO.

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Other records listing Schneider Intl., Ltd. as applicant

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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.