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FDA 510(k)

BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD

K-Number: K903661 · 1990-11-13

ApplicantBruker Medical Imaging, Inc.
Decision Date1990-11-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD is the device name listed in this FDA 510(k) record. The listed applicant is Bruker Medical Imaging, Inc.. It received FDA 510(k) clearance on 1990-11-13 under 510(k) number K903661. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD?

BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is Bruker Medical Imaging, Inc.. The 510(k) number is K903661.

When did BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD receive FDA 510(k) clearance?

BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD received FDA 510(k) clearance on 1990-11-13, under 510(k) number K903661.

Who is the listed applicant for BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD?

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

What is the FDA product code for BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD?

The FDA product code for BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD is LNH.

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Other records listing Bruker Medical Imaging, Inc. as applicant

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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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