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FDA 510(k)

CENTAURI CT SCANNER

K-Number: K840860 · 1984-05-22

ApplicantTechnicare Corp.
Decision Date1984-05-22
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTAURI CT SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1984-05-22 under 510(k) number K840860. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTAURI CT SCANNER?

CENTAURI CT SCANNER is a medical device that received FDA 510(k) clearance on 1984-05-22. The listed applicant is Technicare Corp.. The 510(k) number is K840860.

When did CENTAURI CT SCANNER receive FDA 510(k) clearance?

CENTAURI CT SCANNER received FDA 510(k) clearance on 1984-05-22, under 510(k) number K840860.

Who is the listed applicant for CENTAURI CT SCANNER?

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

What is the FDA product code for CENTAURI CT SCANNER?

The FDA product code for CENTAURI CT SCANNER is JAK.

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Other records listing Technicare Corp. 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.

K854340TECHNICARE 720 HPS CT SCANNERK852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEMK844293AUTO DII MULTI FREQUENCYK844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSK843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-K842777AUTOFOCUS DUAL ELEMENT PROBE

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Related Devices (Code: JAK)

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, 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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