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FDA 510(k)

BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)

K-Number: K903139 · 1990-11-07

ApplicantSiemens Medical Laboratories, Inc.
Decision Date1990-11-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1990-11-07 under 510(k) number K903139. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)?

BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743) is a medical device that received FDA 510(k) clearance on 1990-11-07. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K903139.

When did BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743) receive FDA 510(k) clearance?

BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743) received FDA 510(k) clearance on 1990-11-07, under 510(k) number K903139.

Who is the listed applicant for BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)?

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

What is the FDA product code for BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743)?

The FDA product code for BEAMVIEW & BEAMVIEW PLUS (AKA PROJECT 743) is IYE.

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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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