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FDA 510(k)

DUOFLO 6F

K-Number: K833303 · 1983-12-27

ApplicantArgon Medical Corp.
Decision Date1983-12-27
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DUOFLO 6F is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833303. 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 DUOFLO 6F?

DUOFLO 6F is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Argon Medical Corp.. The 510(k) number is K833303.

When did DUOFLO 6F receive FDA 510(k) clearance?

DUOFLO 6F received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833303.

Who is the listed applicant for DUOFLO 6F?

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

What is the FDA product code for DUOFLO 6F?

The FDA product code for DUOFLO 6F is DQY.

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Other records listing Argon Medical Corp. 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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