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FDA 510(k)

NSK PRECISION APEX LOCATOR (PAL)

K-Number: K053235 · 2006-01-24

Decision Date2006-01-24
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

NSK PRECISION APEX LOCATOR (PAL) is the device name listed in this FDA 510(k) record. The listed applicant is Medicsense USA. It received FDA 510(k) clearance on 2006-01-24 under 510(k) number K053235. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NSK PRECISION APEX LOCATOR (PAL)?

NSK PRECISION APEX LOCATOR (PAL) is a medical device that received FDA 510(k) clearance on 2006-01-24. The listed applicant is Medicsense USA. The 510(k) number is K053235.

When did NSK PRECISION APEX LOCATOR (PAL) receive FDA 510(k) clearance?

NSK PRECISION APEX LOCATOR (PAL) received FDA 510(k) clearance on 2006-01-24, under 510(k) number K053235.

Who is the listed applicant for NSK PRECISION APEX LOCATOR (PAL)?

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

What is the FDA product code for NSK PRECISION APEX LOCATOR (PAL)?

The FDA product code for NSK PRECISION APEX LOCATOR (PAL) is LQY.

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: 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.

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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