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FDA 510(k)

TRANS X 100 CHEST FILM CHANGER

K-Number: K900562 · 1990-04-10

ApplicantAcoma Medical Imaging, Inc.
Decision Date1990-04-10
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRANS X 100 CHEST FILM CHANGER is the device name listed in this FDA 510(k) record. The listed applicant is Acoma Medical Imaging, Inc.. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K900562. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS X 100 CHEST FILM CHANGER?

TRANS X 100 CHEST FILM CHANGER is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Acoma Medical Imaging, Inc.. The 510(k) number is K900562.

When did TRANS X 100 CHEST FILM CHANGER receive FDA 510(k) clearance?

TRANS X 100 CHEST FILM CHANGER received FDA 510(k) clearance on 1990-04-10, under 510(k) number K900562.

Who is the listed applicant for TRANS X 100 CHEST FILM CHANGER?

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

What is the FDA product code for TRANS X 100 CHEST FILM CHANGER?

The FDA product code for TRANS X 100 CHEST FILM CHANGER is KPR.

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Related Devices (Code: KPR)

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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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