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FDA 510(k)

CERVI-TRAC

K-Number: K791808 · 1979-10-01

ApplicantDr. K.G. Rude
Decision Date1979-10-01
Product CodeILZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERVI-TRAC is the device name listed in this FDA 510(k) record. The listed applicant is Dr. K.G. Rude. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791808. The device is classified under product code ILZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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