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FDA 510(k)

COMPUTED DENTAL RADIOGRAPHY

K-Number: K110768 · 2011-04-20

Decision Date2011-04-20
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPUTED DENTAL RADIOGRAPHY is the device name listed in this FDA 510(k) record. The listed applicant is Schick Technologies, Inc.. It received FDA 510(k) clearance on 2011-04-20 under 510(k) number K110768. 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 COMPUTED DENTAL RADIOGRAPHY?

COMPUTED DENTAL RADIOGRAPHY is a medical device that received FDA 510(k) clearance on 2011-04-20. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K110768.

When did COMPUTED DENTAL RADIOGRAPHY receive FDA 510(k) clearance?

COMPUTED DENTAL RADIOGRAPHY received FDA 510(k) clearance on 2011-04-20, under 510(k) number K110768.

Who is the listed applicant for COMPUTED DENTAL RADIOGRAPHY?

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

What is the FDA product code for COMPUTED DENTAL RADIOGRAPHY?

The FDA product code for COMPUTED DENTAL RADIOGRAPHY is MUH.

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 Schick Technologies, Inc. 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.

View all 13 devices →

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.

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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