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FDA 510(k)

ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650

K-Number: K950981 · 1995-04-03

ApplicantBiodex Medical Systems, Inc.
Decision Date1995-04-03
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650 is the device name listed in this FDA 510(k) record. The listed applicant is Biodex Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-04-03 under 510(k) number K950981. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650?

ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650 is a medical device that received FDA 510(k) clearance on 1995-04-03. The listed applicant is Biodex Medical Systems, Inc.. The 510(k) number is K950981.

When did ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650 receive FDA 510(k) clearance?

ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650 received FDA 510(k) clearance on 1995-04-03, under 510(k) number K950981.

Who is the listed applicant for ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650?

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

What is the FDA product code for ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650?

The FDA product code for ULTRA-PRO ULTRASOUND SCANNING TABLE MODEL #056-650 is IXR.

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Other records listing Biodex Medical Systems, Inc. as applicant

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K090296ATOMLAB 400 AND ATOMLAB 500 DOSE CALIBRATORS, MODELS 086-330, -331, -332, -335 AND -336K063666SHARPS CONTAINER, MODEL 039-413K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APK942694STABILITY SYSTEM (110V) MODEL 945-300; STABILITY SYSTEM (220V) MODEL #945-302K940301COMPEX 2K935061LOWER BODY CYCLES

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Related Devices (Code: IXR)

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.

K000412VISION R/F TILTING TABLEVilla Sistemi Medicali S.P.A.K973039LEGACY/LEGACY-D TABLEGE Medical SystemsK971128CAP-35B III/CINE 275Jamieson Film Co.K970640PHILIPS EASY DIAGNOSTPhilips Medical Systems North America, Inc.K965105ELECTROPHYSIOLOGY TILT TABLE MODEL #9660U.S. Imaging Tables, Inc.K965096FLUOROVIEW SERIES FLUOROSCOPIC TABLESU.S. Imaging Tables, Inc.

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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