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FDA 510(k)

ARMSTRONG V VENT TUBE

K-Number: K822375 · 1982-09-09

ApplicantTreace Medical, Inc.
Decision Date1982-09-09
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ARMSTRONG V VENT TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1982-09-09 under 510(k) number K822375. 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 ARMSTRONG V VENT TUBE?

ARMSTRONG V VENT TUBE is a medical device that received FDA 510(k) clearance on 1982-09-09. The listed applicant is Treace Medical, Inc.. The 510(k) number is K822375.

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

ARMSTRONG V VENT TUBE received FDA 510(k) clearance on 1982-09-09, under 510(k) number K822375.

Who is the listed applicant for ARMSTRONG V VENT TUBE?

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

What is the FDA product code for ARMSTRONG V VENT TUBE?

The FDA product code for ARMSTRONG V VENT TUBE is ETD.

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Other records listing Treace Medical, Inc. as applicant

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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Related Devices (Code: ETD)

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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