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FDA 510(k)

CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO

K-Number: K915201 · 1992-07-28

ApplicantBennett X-Ray Corp.
Decision Date1992-07-28
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1992-07-28 under 510(k) number K915201. 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 CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO?

CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO is a medical device that received FDA 510(k) clearance on 1992-07-28. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K915201.

When did CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO receive FDA 510(k) clearance?

CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO received FDA 510(k) clearance on 1992-07-28, under 510(k) number K915201.

Who is the listed applicant for CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO?

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

What is the FDA product code for CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO?

The FDA product code for CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO is IZH.

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Other records listing Bennett X-Ray 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.

K964576PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K952672VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK944978BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK945962BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945731HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORSK945749BENNETT X-RAY TOMOGRAPHY SYSTEM

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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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