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FDA 510(k)

SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA)

K-Number: K911196 · 1991-06-10

ApplicantSchneider Intl., Ltd.
Decision Date1991-06-10
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) 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 1991-06-10 under 510(k) number K911196. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA)?

SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) is a medical device that received FDA 510(k) clearance on 1991-06-10. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K911196.

When did SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) receive FDA 510(k) clearance?

SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) received FDA 510(k) clearance on 1991-06-10, under 510(k) number K911196.

Who is the listed applicant for SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA)?

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 TOTAL CROSS .021 PERCU TRANS ANGIO (PTA)?

The FDA product code for SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA) is LIT.

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Other records listing Schneider Intl., Ltd. as applicant

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Related Devices (Code: LIT)

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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