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FDA 510(k)

ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0

K-Number: K992352 · 1999-09-29

ApplicantInteleradiology, Inc.
Decision Date1999-09-29
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Inteleradiology, Inc.. It received FDA 510(k) clearance on 1999-09-29 under 510(k) number K992352. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0?

ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 is a medical device that received FDA 510(k) clearance on 1999-09-29. The listed applicant is Inteleradiology, Inc.. The 510(k) number is K992352.

When did ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 receive FDA 510(k) clearance?

ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 received FDA 510(k) clearance on 1999-09-29, under 510(k) number K992352.

Who is the listed applicant for ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0?

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

What is the FDA product code for ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0?

The FDA product code for ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0 is LMD.

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Related Devices (Code: LMD)

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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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