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FDA 510(k)

AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR)

K-Number: K961023 · 1996-09-09

ApplicantAccuimage, Inc.
Decision Date1996-09-09
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR) is the device name listed in this FDA 510(k) record. The listed applicant is Accuimage, Inc.. It received FDA 510(k) clearance on 1996-09-09 under 510(k) number K961023. 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 AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR)?

AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR) is a medical device that received FDA 510(k) clearance on 1996-09-09. The listed applicant is Accuimage, Inc.. The 510(k) number is K961023.

When did AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR) receive FDA 510(k) clearance?

AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR) received FDA 510(k) clearance on 1996-09-09, under 510(k) number K961023.

Who is the listed applicant for AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR)?

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

What is the FDA product code for AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR)?

The FDA product code for AIDP(ACCUIMAGE IMAGE DISPLAY PROCESSOR) is LMD.

Related Clinical Trials

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Related Devices (Code: LMD)

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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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