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FDA 510(k)

VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS

K-Number: K910111 · 1991-09-23

ApplicantInstrumentarium Imaging, Inc.
Decision Date1991-09-23
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Imaging, Inc.. It received FDA 510(k) clearance on 1991-09-23 under 510(k) number K910111. 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 VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS?

VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Instrumentarium Imaging, Inc.. The 510(k) number is K910111.

When did VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS receive FDA 510(k) clearance?

VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS received FDA 510(k) clearance on 1991-09-23, under 510(k) number K910111.

Who is the listed applicant for VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS?

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

What is the FDA product code for VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS?

The FDA product code for VARIOUS MODELS OF DAYLIGHT CASSETTE HOLDERS is IZH.

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Other records listing Instrumentarium Imaging, 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.

K002472DELTA 32 AND DELTA 32 TACTK001928SIGMAK000976DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)K001171DELTA 16 TACTK973642ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100K955411DELTA 16

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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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