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FDA 510(k)

EMI SIMULATOR REMOTE CONTROL CONSOLE

K-Number: K781519 · 1978-09-14

ApplicantEmi Medical, Inc.
Decision Date1978-09-14
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EMI SIMULATOR REMOTE CONTROL CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is Emi Medical, Inc.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781519. 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 EMI SIMULATOR REMOTE CONTROL CONSOLE?

EMI SIMULATOR REMOTE CONTROL CONSOLE is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Emi Medical, Inc.. The 510(k) number is K781519.

When did EMI SIMULATOR REMOTE CONTROL CONSOLE receive FDA 510(k) clearance?

EMI SIMULATOR REMOTE CONTROL CONSOLE received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781519.

Who is the listed applicant for EMI SIMULATOR REMOTE CONTROL CONSOLE?

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

What is the FDA product code for EMI SIMULATOR REMOTE CONTROL CONSOLE?

The FDA product code for EMI SIMULATOR REMOTE CONTROL CONSOLE is KPQ.

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Other records listing Emi Medical, 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.

K791429EMISONIC 4290K781936SCANNER-EMI 7020 AND 7020RK781051EMISONIC 4201K780995COMPUTERIZED AXIAL TOMOGRAPHYK780928CT5137 HIGH RESOLUTION OPTIONK7809305543 INDEPENDENT VIEWING 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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