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FDA 510(k)

ADVANCED AUTOMATIC KV

K-Number: K934831 · 1994-08-23

ApplicantElscint, Inc.
Decision Date1994-08-23
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANCED AUTOMATIC KV is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K934831. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED AUTOMATIC KV?

ADVANCED AUTOMATIC KV is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Elscint, Inc.. The 510(k) number is K934831.

When did ADVANCED AUTOMATIC KV receive FDA 510(k) clearance?

ADVANCED AUTOMATIC KV received FDA 510(k) clearance on 1994-08-23, under 510(k) number K934831.

Who is the listed applicant for ADVANCED AUTOMATIC KV?

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 ADVANCED AUTOMATIC KV?

The FDA product code for ADVANCED AUTOMATIC KV is IZH.

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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)

View all 94 devices →

Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, 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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