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FDA 510(k)

NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM

K-Number: K931410 · 1994-02-18

ApplicantNovus Technologies, Inc.
Decision Date1994-02-18
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Novus Technologies, Inc.. It received FDA 510(k) clearance on 1994-02-18 under 510(k) number K931410. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM?

NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Novus Technologies, Inc.. The 510(k) number is K931410.

When did NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM receive FDA 510(k) clearance?

NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM received FDA 510(k) clearance on 1994-02-18, under 510(k) number K931410.

Who is the listed applicant for NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM?

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

What is the FDA product code for NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM?

The FDA product code for NOVUS IMAGE ARCHIVE SYSTEM, TELERADIOLOGY SYSTEM is LMB.

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Related Devices (Code: LMB)

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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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