FDA 510(k)

CDR PANX, MODEL 4792

K-Number: K031291 · 2003-05-05

Decision Date2003-05-05

Product CodeMUH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CDR PANX, MODEL 4792 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 2003-05-05 under 510(k) number K031291. 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 CDR PANX, MODEL 4792?

CDR PANX, MODEL 4792 is a medical device that received FDA 510(k) clearance on 2003-05-05. The listed applicant is Schick Technologies, Inc.. The 510(k) number is K031291.

When did CDR PANX, MODEL 4792 receive FDA 510(k) clearance?

CDR PANX, MODEL 4792 received FDA 510(k) clearance on 2003-05-05, under 510(k) number K031291.

Who is the listed applicant for CDR PANX, MODEL 4792?

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 CDR PANX, MODEL 4792?

The FDA product code for CDR PANX, MODEL 4792 is MUH.

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Other records listing Schick Technologies, Inc. as applicant

K110768COMPUTED DENTAL RADIOGRAPHY K093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM K072134SCHICK COMPUTED ORAL RADIOLOGY SYSTEM K053558CEPH, MODEL 4900 K041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM K022953MODIFICATION 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.