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FDA 510(k)

RADKOR TS10-B

K-Number: K892196 · 1989-04-26

ApplicantRadkor, Inc.
Decision Date1989-04-26
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADKOR TS10-B is the device name listed in this FDA 510(k) record. The listed applicant is Radkor, Inc.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K892196. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADKOR TS10-B?

RADKOR TS10-B is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Radkor, Inc.. The 510(k) number is K892196.

When did RADKOR TS10-B receive FDA 510(k) clearance?

RADKOR TS10-B received FDA 510(k) clearance on 1989-04-26, under 510(k) number K892196.

Who is the listed applicant for RADKOR TS10-B?

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

What is the FDA product code for RADKOR TS10-B?

The FDA product code for RADKOR TS10-B is IXQ.

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Other records listing Radkor, 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.

K895969RADKOR DXG-650RK891395RADKOR BS-10 AND BS-10TK883864RADKOR SFR-70K883885RADKOR, RF-159K881701RADKOR SFC-21K881696RADKOR XG-325

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Related Devices (Code: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, 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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