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FDA 510(k)

CANNON II PLUS

K-Number: K040078 · 2004-02-13

ApplicantArrow International, Inc.
Decision Date2004-02-13
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

CANNON II PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc.. It received FDA 510(k) clearance on 2004-02-13 under 510(k) number K040078. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CANNON II PLUS?

CANNON II PLUS is a medical device that received FDA 510(k) clearance on 2004-02-13. The listed applicant is Arrow International, Inc.. The 510(k) number is K040078.

When did CANNON II PLUS receive FDA 510(k) clearance?

CANNON II PLUS received FDA 510(k) clearance on 2004-02-13, under 510(k) number K040078.

Who is the listed applicant for CANNON II PLUS?

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

What is the FDA product code for CANNON II PLUS?

The FDA product code for CANNON II PLUS is MSD.

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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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