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FDA 510(k)

APEX HRI DIGITAL RADIOGRAPHY SYSTEM

K-Number: K023292 · 2002-12-13

ApplicantKrugman Technologies, Inc.
Decision Date2002-12-13
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APEX HRI DIGITAL RADIOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Krugman Technologies, Inc.. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K023292. 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 APEX HRI DIGITAL RADIOGRAPHY SYSTEM?

APEX HRI DIGITAL RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Krugman Technologies, Inc.. The 510(k) number is K023292.

When did APEX HRI DIGITAL RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

APEX HRI DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023292.

Who is the listed applicant for APEX HRI DIGITAL RADIOGRAPHY SYSTEM?

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

What is the FDA product code for APEX HRI DIGITAL RADIOGRAPHY SYSTEM?

The FDA product code for APEX HRI DIGITAL RADIOGRAPHY SYSTEM is MUH.

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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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