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FDA 510(k)

ZINETICS GASTROMETER (TM)

K-Number: K862727 · 1986-11-19

ApplicantZinetics Medical Technology Corp.
Decision Date1986-11-19
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZINETICS GASTROMETER (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Zinetics Medical Technology Corp.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K862727. 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 GASTROMETER (TM)?

ZINETICS GASTROMETER (TM) is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Zinetics Medical Technology Corp.. The 510(k) number is K862727.

When did ZINETICS GASTROMETER (TM) receive FDA 510(k) clearance?

ZINETICS GASTROMETER (TM) received FDA 510(k) clearance on 1986-11-19, under 510(k) number K862727.

Who is the listed applicant for ZINETICS GASTROMETER (TM)?

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

What is the FDA product code for ZINETICS GASTROMETER (TM)?

The FDA product code for ZINETICS GASTROMETER (TM) is FFT.

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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.

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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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