VERI/TRODES
K-Number: K770323 · 1977-02-28
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Device Summary
Frequently Asked Questions
What is the VERI/TRODES?
VERI/TRODES is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Verite Scientific, Inc.. The 510(k) number is K770323.
When did VERI/TRODES receive FDA 510(k) clearance?
VERI/TRODES received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770323.
Who is the listed applicant for VERI/TRODES?
The FDA 510(k) record lists Verite Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERI/TRODES?
The FDA product code for VERI/TRODES is GXY.
Related Clinical Trials
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.
Other records listing Verite Scientific, 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.
Related Devices (Code: GXY)
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.
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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