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FDA 510(k)

CEPH, MODEL 4900

K-Number: K053558 · 2006-02-17

ApplicantSchick Technologies, Inc.
Decision Date2006-02-17
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEPH, MODEL 4900 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 2006-02-17 under 510(k) number K053558. 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 CEPH, MODEL 4900?

CEPH, MODEL 4900 is a medical device that received FDA 510(k) clearance on 2006-02-17. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K053558.

When did CEPH, MODEL 4900 receive FDA 510(k) clearance?

CEPH, MODEL 4900 received FDA 510(k) clearance on 2006-02-17, under 510(k) number K053558.

Who is the listed applicant for CEPH, MODEL 4900?

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 CEPH, MODEL 4900?

The FDA product code for CEPH, MODEL 4900 is MUH.

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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.

K110768COMPUTED DENTAL RADIOGRAPHYK093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK072134SCHICK COMPUTED ORAL RADIOLOGY SYSTEMK041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMK031291CDR PANX, MODEL 4792K022953MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM

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Related Devices (Code: MUH)

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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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