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FDA 510(k)

ARCHIVEMANAGER

K-Number: K950513 · 1995-11-13

ApplicantCemax, Inc.
Decision Date1995-11-13
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARCHIVEMANAGER is the device name listed in this FDA 510(k) record. The listed applicant is Cemax, Inc.. It received FDA 510(k) clearance on 1995-11-13 under 510(k) number K950513. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARCHIVEMANAGER?

ARCHIVEMANAGER is a medical device that received FDA 510(k) clearance on 1995-11-13. The listed applicant is Cemax, Inc.. The 510(k) number is K950513.

When did ARCHIVEMANAGER receive FDA 510(k) clearance?

ARCHIVEMANAGER received FDA 510(k) clearance on 1995-11-13, under 510(k) number K950513.

Who is the listed applicant for ARCHIVEMANAGER?

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

What is the FDA product code for ARCHIVEMANAGER?

The FDA product code for ARCHIVEMANAGER is LMD.

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Other records listing Cemax, 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.

K945188CEMAX VIPSTATION AND/OR SOFTWAREK943357CEMAX SCANLINK VK932371CEMAX CLINICALVIEW(TM) STATION AND/OR SOFTWAREK932372CEMAX VIPSTATION(TM) AND/OR SOFTWAREK905801CEMAX SPARCSTATION IMAGING SOFTWARE AND WORKSTATIOK880169CEMAX 5000 MULTIDIMENSIONAL IMAGING WORKSTATION

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Related Devices (Code: LMD)

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K994329IIVS INTEGRATED IMAGE VIEWING STATIONTerarecon,Inc.K992698STENTOR, PAGEVIEWStentor, Inc.K992426RAYPAX WEB CLINICAL SYSTEMSamsung Sds Co., Ltd.K992352ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0Inteleradiology, Inc.K991537SAMSUNG RAYPAX SYSTEMSamsung Sds Co., Ltd.K984000STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEMSurgical Navigation Technologies, 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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