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FDA 510(k)

IMAGEVIEW 46000

K-Number: K925265 · 1993-06-09

ApplicantCanberra Industries, Inc.
Decision Date1993-06-09
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGEVIEW 46000 is the device name listed in this FDA 510(k) record. The listed applicant is Canberra Industries, Inc.. It received FDA 510(k) clearance on 1993-06-09 under 510(k) number K925265. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGEVIEW 46000?

IMAGEVIEW 46000 is a medical device that received FDA 510(k) clearance on 1993-06-09. The listed applicant is Canberra Industries, Inc.. The 510(k) number is K925265.

When did IMAGEVIEW 46000 receive FDA 510(k) clearance?

IMAGEVIEW 46000 received FDA 510(k) clearance on 1993-06-09, under 510(k) number K925265.

Who is the listed applicant for IMAGEVIEW 46000?

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

What is the FDA product code for IMAGEVIEW 46000?

The FDA product code for IMAGEVIEW 46000 is LMC.

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Other records listing Canberra Industries, 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.

K896202MATRIX(TM)-96K834168FIBRINOGEN UPTAKE SYS -VARIOUS MODELS

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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