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FDA 510(k)

TRI AUTO ZX

K-Number: K970339 · 1997-06-04

ApplicantJ. Morita USA, Inc.
Decision Date1997-06-04
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRI AUTO ZX is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 1997-06-04 under 510(k) number K970339. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRI AUTO ZX?

TRI AUTO ZX is a medical device that received FDA 510(k) clearance on 1997-06-04. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K970339.

When did TRI AUTO ZX receive FDA 510(k) clearance?

TRI AUTO ZX received FDA 510(k) clearance on 1997-06-04, under 510(k) number K970339.

Who is the listed applicant for TRI AUTO ZX?

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

What is the FDA product code for TRI AUTO ZX?

The FDA product code for TRI AUTO ZX is EKX.

Other records listing J. Morita USA, 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.

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Related Devices (Code: EKX)

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.

K261987Reusable SmartPegOsstell ABK252223Alpha Endo Handpiece (Alpha Endo)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K251597InnerView SystemPerimetrics, Inc.K243692EnDrive (EnDriveUS)Advanced Technology Research (A.T.R.) S.R.L.K242514Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)Shenzhen Rogin Medical Co., Ltd.K241065ChecQ (AC100)Dentis Co., Ltd.

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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