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FDA 510(k)

PULPDENT CANAL FINDER

K-Number: K945811 · 1995-01-20

Decision Date1995-01-20
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

PULPDENT CANAL FINDER is the device name listed in this FDA 510(k) record. The listed applicant is Pulpdent Corp.. It received FDA 510(k) clearance on 1995-01-20 under 510(k) number K945811. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULPDENT CANAL FINDER?

PULPDENT CANAL FINDER is a medical device that received FDA 510(k) clearance on 1995-01-20. The listed applicant is Pulpdent Corp.. The 510(k) number is K945811.

When did PULPDENT CANAL FINDER receive FDA 510(k) clearance?

PULPDENT CANAL FINDER received FDA 510(k) clearance on 1995-01-20, under 510(k) number K945811.

Who is the listed applicant for PULPDENT CANAL FINDER?

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

What is the FDA product code for PULPDENT CANAL FINDER?

The FDA product code for PULPDENT CANAL FINDER 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.

Other records listing Pulpdent Corp. 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: 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

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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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