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FDA 510(k)

OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM

K-Number: K901118 · 1990-04-10

ApplicantAdac Laboratories
Decision Date1990-04-10
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K901118. 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 OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM?

OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Adac Laboratories. The 510(k) number is K901118.

When did OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM receive FDA 510(k) clearance?

OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM received FDA 510(k) clearance on 1990-04-10, under 510(k) number K901118.

Who is the listed applicant for OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM?

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

What is the FDA product code for OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM?

The FDA product code for OMNIVIEW DIGITAL RADIOLOGY IMAGING SYSTEM is LMB.

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Other records listing Adac Laboratories as applicant

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K062298APOLLO GAMMA CAMERA SYSTEMK061029JETSTREAM WORKSPACEK060020AUTOQUANT PLUSK051351PRECEDENCE SPECT/CT IMAGING SYSTEMK042880JETSTREAM WORKSPACEK042903AUTOSPECS

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Related Devices (Code: LMB)

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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.

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