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FDA 510(k)

CMS RECORD AND VERIFY

K-Number: K921108 · 1992-11-02

ApplicantComputerized Medical Systems, Inc.
Decision Date1992-11-02
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CMS RECORD AND VERIFY is the device name listed in this FDA 510(k) record. The listed applicant is Computerized Medical Systems, Inc.. It received FDA 510(k) clearance on 1992-11-02 under 510(k) number K921108. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMS RECORD AND VERIFY?

CMS RECORD AND VERIFY is a medical device that received FDA 510(k) clearance on 1992-11-02. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K921108.

When did CMS RECORD AND VERIFY receive FDA 510(k) clearance?

CMS RECORD AND VERIFY received FDA 510(k) clearance on 1992-11-02, under 510(k) number K921108.

Who is the listed applicant for CMS RECORD AND VERIFY?

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

What is the FDA product code for CMS RECORD AND VERIFY?

The FDA product code for CMS RECORD AND VERIFY is KPQ.

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Other records listing Computerized Medical Systems, Inc. as applicant

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K110730MONACO RTP SYSTEMK102216XIO RTP SYSTEMK092132XIO RTP SYSTEMK091179MONACO RTP SYSTEM, VMAT OPTIONK080799ATLAS-BASED AUTOSEGMENTATIONK071938MONACO RTP SYSTEM

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Related Devices (Code: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, LLC

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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