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FDA 510(k)

CLEARTOOTH DIGITAL X-RAY SYSTEM

K-Number: K033147 · 2003-12-30

ApplicantCleartooth Electronics, Inc.
Decision Date2003-12-30
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEARTOOTH DIGITAL X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cleartooth Electronics, Inc.. It received FDA 510(k) clearance on 2003-12-30 under 510(k) number K033147. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARTOOTH DIGITAL X-RAY SYSTEM?

CLEARTOOTH DIGITAL X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-30. The listed applicant is Cleartooth Electronics, Inc.. The 510(k) number is K033147.

When did CLEARTOOTH DIGITAL X-RAY SYSTEM receive FDA 510(k) clearance?

CLEARTOOTH DIGITAL X-RAY SYSTEM received FDA 510(k) clearance on 2003-12-30, under 510(k) number K033147.

Who is the listed applicant for CLEARTOOTH DIGITAL X-RAY SYSTEM?

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

What is the FDA product code for CLEARTOOTH DIGITAL X-RAY SYSTEM?

The FDA product code for CLEARTOOTH DIGITAL X-RAY SYSTEM is MUH.

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Related Devices (Code: MUH)

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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