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FDA 510(k)

ROOT CANAL LENGTH MEASURING DEVICE

K-Number: K953867 · 1995-12-01

ApplicantJ. Morita USA, Inc.
Decision Date1995-12-01
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

ROOT CANAL LENGTH MEASURING DEVICE 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 1995-12-01 under 510(k) number K953867. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROOT CANAL LENGTH MEASURING DEVICE?

ROOT CANAL LENGTH MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1995-12-01. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K953867.

When did ROOT CANAL LENGTH MEASURING DEVICE receive FDA 510(k) clearance?

ROOT CANAL LENGTH MEASURING DEVICE received FDA 510(k) clearance on 1995-12-01, under 510(k) number K953867.

Who is the listed applicant for ROOT CANAL LENGTH MEASURING DEVICE?

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 ROOT CANAL LENGTH MEASURING DEVICE?

The FDA product code for ROOT CANAL LENGTH MEASURING DEVICE is LQY.

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Other records listing J. Morita USA, Inc. as applicant

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Related Devices (Code: LQY)

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

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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