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FDA 510(k)

PHILIPS SITE VIEW WORKSTATION

K-Number: K960809 · 1996-04-07

ApplicantPhilips Medical Systems North America, Inc.
Decision Date1996-04-07
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS SITE VIEW WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 1996-04-07 under 510(k) number K960809. 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 PHILIPS SITE VIEW WORKSTATION?

PHILIPS SITE VIEW WORKSTATION is a medical device that received FDA 510(k) clearance on 1996-04-07. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K960809.

When did PHILIPS SITE VIEW WORKSTATION receive FDA 510(k) clearance?

PHILIPS SITE VIEW WORKSTATION received FDA 510(k) clearance on 1996-04-07, under 510(k) number K960809.

Who is the listed applicant for PHILIPS SITE VIEW WORKSTATION?

The FDA 510(k) record lists Philips Medical Systems North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS SITE VIEW WORKSTATION?

The FDA product code for PHILIPS SITE VIEW WORKSTATION is LMD.

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Other records listing Philips Medical Systems North America, 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.

K102005ALLURA XPER OR TABLE SERIESK062233HEARTSTART MRX MONITOR/DEFIBRILLATORK062283THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORSK061052THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90K050151MULTIDIAGNOST ELEVAK042867PHILIPS ORTHOPAEDIC APPLICATIONS

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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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