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FDA 510(k)

GUIDING CATHETER HEMOSTASIS VALVE CAP

K-Number: K933033 · 1993-09-10

ApplicantArrow Intl., Inc.
Decision Date1993-09-10
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GUIDING CATHETER HEMOSTASIS VALVE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1993-09-10 under 510(k) number K933033. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDING CATHETER HEMOSTASIS VALVE CAP?

GUIDING CATHETER HEMOSTASIS VALVE CAP is a medical device that received FDA 510(k) clearance on 1993-09-10. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K933033.

When did GUIDING CATHETER HEMOSTASIS VALVE CAP receive FDA 510(k) clearance?

GUIDING CATHETER HEMOSTASIS VALVE CAP received FDA 510(k) clearance on 1993-09-10, under 510(k) number K933033.

Who is the listed applicant for GUIDING CATHETER HEMOSTASIS VALVE CAP?

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

What is the FDA product code for GUIDING CATHETER HEMOSTASIS VALVE CAP?

The FDA product code for GUIDING CATHETER HEMOSTASIS VALVE CAP is DQY.

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Other records listing Arrow Intl., Inc. as applicant

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Related Devices (Code: DQY)

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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