FDA 510(k)

ARGON CONTINUOUS FLUSH DEVICE

K-Number: K070384 · 2007-03-29

Decision Date2007-03-29

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ARGON CONTINUOUS FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2007-03-29 under 510(k) number K070384. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON CONTINUOUS FLUSH DEVICE?

ARGON CONTINUOUS FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 2007-03-29. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K070384.

When did ARGON CONTINUOUS FLUSH DEVICE receive FDA 510(k) clearance?

ARGON CONTINUOUS FLUSH DEVICE received FDA 510(k) clearance on 2007-03-29, under 510(k) number K070384.

Who is the listed applicant for ARGON CONTINUOUS FLUSH DEVICE?

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

What is the FDA product code for ARGON CONTINUOUS FLUSH DEVICE?

The FDA product code for ARGON CONTINUOUS FLUSH DEVICE is KRA.

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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.