FDA 510(k)

MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE

K-Number: K902005 · 1990-09-20

Decision Date1990-09-20

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Omega Medical Imaging, Inc.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K902005. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE?

MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Omega Medical Imaging, Inc.. The 510(k) number is K902005.

When did MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE receive FDA 510(k) clearance?

MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902005.

Who is the listed applicant for MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE?

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

What is the FDA product code for MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE?

The FDA product code for MODEL B-200 C-ARM & MODEL C-300 CARDIAC TABLE is JAA.

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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.