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FDA 510(k)

VISIONLINK DICOM MODULE

K-Number: K942860 · 1994-09-16

ApplicantEvergreen Technologies, Inc.
Decision Date1994-09-16
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISIONLINK DICOM MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Evergreen Technologies, Inc.. It received FDA 510(k) clearance on 1994-09-16 under 510(k) number K942860. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISIONLINK DICOM MODULE?

VISIONLINK DICOM MODULE is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is Evergreen Technologies, Inc.. The 510(k) number is K942860.

When did VISIONLINK DICOM MODULE receive FDA 510(k) clearance?

VISIONLINK DICOM MODULE received FDA 510(k) clearance on 1994-09-16, under 510(k) number K942860.

Who is the listed applicant for VISIONLINK DICOM MODULE?

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

What is the FDA product code for VISIONLINK DICOM MODULE?

The FDA product code for VISIONLINK DICOM MODULE is KPS.

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Other records listing Evergreen Technologies, 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.

K942861MEDVISION ENVIROMENT/MEDVISION 2.0K935103VISIONLINK ACR-NEMA CONVERSION UTILITIESK933372VISIONLINK INTERFILE CONVERSION SOFTWAREK933209VISIONTOOLK924178MEDVISION(TM) IMAGING SOFTWAREK921484MEDVISION

View all 7 devices →

Related Devices (Code: KPS)

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.

K261305MICSI-PETMicrostructure Imaging, Inc.K261427uMI Panvivo (uMI Panvivo M)Shanghai United Imaging Healthcare Co., Ltd.K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 FamilySiemens Medical Solutions USA, Inc.K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)Spectrum Dynamics Medical, Ltd.

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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