FDA 510(k)

DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR

K-Number: K983392 · 1998-12-15

Decision Date1998-12-15

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Data Ray. It received FDA 510(k) clearance on 1998-12-15 under 510(k) number K983392. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR?

DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR is a medical device that received FDA 510(k) clearance on 1998-12-15. The listed applicant is Data Ray. The 510(k) number is K983392.

When did DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR receive FDA 510(k) clearance?

DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR received FDA 510(k) clearance on 1998-12-15, under 510(k) number K983392.

Who is the listed applicant for DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR?

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

What is the FDA product code for DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR?

The FDA product code for DATA RAY CORPORATION DR11021 MEDICAL IMAGING MONITOR is LLZ.

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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.