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FDA 510(k)

DENTOOL

K-Number: K923780 · 1995-03-21

ApplicantDentool, Inc.
Decision Date1995-03-21
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTOOL is the device name listed in this FDA 510(k) record. The listed applicant is Dentool, Inc.. It received FDA 510(k) clearance on 1995-03-21 under 510(k) number K923780. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTOOL?

DENTOOL is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Dentool, Inc.. The 510(k) number is K923780.

When did DENTOOL receive FDA 510(k) clearance?

DENTOOL received FDA 510(k) clearance on 1995-03-21, under 510(k) number K923780.

Who is the listed applicant for DENTOOL?

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

What is the FDA product code for DENTOOL?

The FDA product code for DENTOOL is EFB.

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: EFB)

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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