FDA 510(k)

CODEMASTER XL + XL W/SHOCK ADVISORY OPTION

K-Number: K954957 · 1996-05-07

Decision Date1996-05-07

Product CodeMKJ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CODEMASTER XL + XL W/SHOCK ADVISORY OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1996-05-07 under 510(k) number K954957. The device is classified under product code MKJ. It was reviewed by the CV advisory panel. Product code MKJ falls under the category of Dental, which includes dental instruments, materials, and equipment. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODEMASTER XL + XL W/SHOCK ADVISORY OPTION?

CODEMASTER XL + XL W/SHOCK ADVISORY OPTION is a medical device that received FDA 510(k) clearance on 1996-05-07. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K954957.

When did CODEMASTER XL + XL W/SHOCK ADVISORY OPTION receive FDA 510(k) clearance?

CODEMASTER XL + XL W/SHOCK ADVISORY OPTION received FDA 510(k) clearance on 1996-05-07, under 510(k) number K954957.

Who is the listed applicant for CODEMASTER XL + XL W/SHOCK ADVISORY OPTION?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODEMASTER XL + XL W/SHOCK ADVISORY OPTION?

The FDA product code for CODEMASTER XL + XL W/SHOCK ADVISORY OPTION is MKJ. This falls under the Dental category.

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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.