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FDA 510(k)

9600 FLUOROSCOPIC IMAGING SYSTEM

K-Number: K926056 · 1993-01-21

ApplicantOec-Diasonics, Inc.
Decision Date1993-01-21
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

9600 FLUOROSCOPIC IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oec-Diasonics, Inc.. It received FDA 510(k) clearance on 1993-01-21 under 510(k) number K926056. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 9600 FLUOROSCOPIC IMAGING SYSTEM?

9600 FLUOROSCOPIC IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Oec-Diasonics, Inc.. The 510(k) number is K926056.

When did 9600 FLUOROSCOPIC IMAGING SYSTEM receive FDA 510(k) clearance?

9600 FLUOROSCOPIC IMAGING SYSTEM received FDA 510(k) clearance on 1993-01-21, under 510(k) number K926056.

Who is the listed applicant for 9600 FLUOROSCOPIC IMAGING SYSTEM?

The FDA 510(k) record lists Oec-Diasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 9600 FLUOROSCOPIC IMAGING SYSTEM?

The FDA product code for 9600 FLUOROSCOPIC IMAGING SYSTEM is OXO.

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Other records listing Oec-Diasonics, 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.

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Related Devices (Code: OXO)

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.

K253296Digital C-ARM with 3DAllengers Medical Systems LimitedK252579Orthoscan TAU MVP Mini C-Arm SystemZiehm-Orthoscan, Inc.K253269OEC One CFDGe Hualun Medical Systems Co. , Ltd.K251004Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)Hefei Chimed Intelligent Machine Co., Ltd.K250587Orthoscan TAU Mini C-ArmZiehm-Orthoscan, Inc.K243452Orthoscan VERSA Mini C-ArmZiehm-Orthoscan, 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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