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FDA 510(k)

UNIFLOW VENT TUBE

K-Number: K842637 · 1984-10-25

ApplicantRichards Medical Co., Inc.
Decision Date1984-10-25
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

UNIFLOW VENT TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K842637. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIFLOW VENT TUBE?

UNIFLOW VENT TUBE is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K842637.

When did UNIFLOW VENT TUBE receive FDA 510(k) clearance?

UNIFLOW VENT TUBE received FDA 510(k) clearance on 1984-10-25, under 510(k) number K842637.

Who is the listed applicant for UNIFLOW VENT TUBE?

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

What is the FDA product code for UNIFLOW VENT TUBE?

The FDA product code for UNIFLOW VENT TUBE is ETD.

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Other records listing Richards Medical Co., Inc. as applicant

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Related Devices (Code: ETD)

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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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