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FDA 510(k)

ZINETICS INTERNAL REFERENCE PROBE

K-Number: K910694 · 1991-05-17

Decision Date1991-05-17
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZINETICS INTERNAL REFERENCE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Zinetics Medical, Inc.. It received FDA 510(k) clearance on 1991-05-17 under 510(k) number K910694. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZINETICS INTERNAL REFERENCE PROBE?

ZINETICS INTERNAL REFERENCE PROBE is a medical device that received FDA 510(k) clearance on 1991-05-17. The listed applicant is Zinetics Medical, Inc.. The 510(k) number is K910694.

When did ZINETICS INTERNAL REFERENCE PROBE receive FDA 510(k) clearance?

ZINETICS INTERNAL REFERENCE PROBE received FDA 510(k) clearance on 1991-05-17, under 510(k) number K910694.

Who is the listed applicant for ZINETICS INTERNAL REFERENCE PROBE?

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

What is the FDA product code for ZINETICS INTERNAL REFERENCE PROBE?

The FDA product code for ZINETICS INTERNAL REFERENCE PROBE is FFT.

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 Zinetics 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.

Related Devices (Code: FFT)

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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