CERVI-TRAC
K-Number: K791808 · 1979-10-01
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Device Summary
Frequently Asked Questions
What is the CERVI-TRAC?
CERVI-TRAC is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Dr. K.G. Rude. The 510(k) number is K791808.
When did CERVI-TRAC receive FDA 510(k) clearance?
CERVI-TRAC received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791808.
Who is the listed applicant for CERVI-TRAC?
The FDA 510(k) record lists Dr. K.G. Rude as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERVI-TRAC?
The FDA product code for CERVI-TRAC is ILZ.
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.
Related Devices (Code: ILZ)
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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