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FDA 510(k)

ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW

K-Number: K932508 · 1994-07-29

ApplicantElscint, Inc.
Decision Date1994-07-29
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1994-07-29 under 510(k) number K932508. 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 ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW?

ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Elscint, Inc.. The 510(k) number is K932508.

When did ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW receive FDA 510(k) clearance?

ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW received FDA 510(k) clearance on 1994-07-29, under 510(k) number K932508.

Who is the listed applicant for ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW?

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

What is the FDA product code for ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW?

The FDA product code for ANGIOCT OPTION FOR CT-TWIN, HELICAT & OMNIVIEW is JAK.

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Other records listing Elscint, 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.

K983313ADVANCED AUTOMATIC DETECTOR SELECTION OPTION FOR GLORYK982060VOLUMAX CT IMAGING SYSTEMK974344CT SCOPEK980306GYREX 2T PRESTIGE, GYREX PRIMA ITG, GYREX PRIVILEGE, GYREX V-EPK974614GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA 1TG 100-6250-0102K9725922T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)

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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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