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FDA 510(k)

SYMPHONY 360 REMOTE CONTROL TABLE

K-Number: K981227 · 1998-06-30

ApplicantAcoma Medical Imaging, Inc.
Decision Date1998-06-30
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYMPHONY 360 REMOTE CONTROL TABLE 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 1998-06-30 under 510(k) number K981227. 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 SYMPHONY 360 REMOTE CONTROL TABLE?

SYMPHONY 360 REMOTE CONTROL TABLE is a medical device that received FDA 510(k) clearance on 1998-06-30. The listed applicant is Acoma Medical Imaging, Inc.. The 510(k) number is K981227.

When did SYMPHONY 360 REMOTE CONTROL TABLE receive FDA 510(k) clearance?

SYMPHONY 360 REMOTE CONTROL TABLE received FDA 510(k) clearance on 1998-06-30, under 510(k) number K981227.

Who is the listed applicant for SYMPHONY 360 REMOTE CONTROL TABLE?

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 SYMPHONY 360 REMOTE CONTROL TABLE?

The FDA product code for SYMPHONY 360 REMOTE CONTROL TABLE is JAA.

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Other records listing Acoma Medical Imaging, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981131PATHFINDER MOBILE C ARMK963851TILTING RADIOGRAPHIC TABLE (REMOTE)K944952ANGIOGRAPHIC SYSTEMK941004CTS SYSTEMK941017F/C/W TUBESTANDK925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGER

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Related Devices (Code: JAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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