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FDA 510(k)

MULTIDOS, QC6PLUS

K-Number: K972211 · 1997-09-10

ApplicantPtw-New York Corp.
Decision Date1997-09-10
Product CodeLHN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIDOS, QC6PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Ptw-New York Corp.. It received FDA 510(k) clearance on 1997-09-10 under 510(k) number K972211. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIDOS, QC6PLUS?

MULTIDOS, QC6PLUS is a medical device that received FDA 510(k) clearance on 1997-09-10. The listed applicant is Ptw-New York Corp.. The 510(k) number is K972211.

When did MULTIDOS, QC6PLUS receive FDA 510(k) clearance?

MULTIDOS, QC6PLUS received FDA 510(k) clearance on 1997-09-10, under 510(k) number K972211.

Who is the listed applicant for MULTIDOS, QC6PLUS?

The FDA 510(k) record lists Ptw-New York Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIDOS, QC6PLUS?

The FDA product code for MULTIDOS, QC6PLUS is LHN.

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Other records listing Ptw-New York Corp. 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.

K062817PTW DAVID IMRT QC VERIFICATION SYSTEMK010705OPTIDOSK010916PTW DOSIMETRY DIODE, T60008K9722120.015CC PINPOINT IONIZATION CHAMBER, 0.005 CC PINPOINT IONIZATION CHAMBERK9612080.6CC IONIZATION CHAMBER - WATERPROOF 0.6CC IONIZATION CHAMBERK954165PTW-MP3 & PTW-MP3S AUTOMATIC WATER PHANTOM

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Related Devices (Code: LHN)

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.

K260597VIRTUE QAProNova SolutionsK260174PROBEAT-CRHitachi High-Tech Corp.K252815ProBeam 360 Proton Therapy System v3.0Varian Medical Systems, Inc.K253406S250-FIT Proton Beam Radiation Therapy Device (S250-FIT)Mevion Medical Systems, Inc.K250986S250-FIT Proton Beam Radiation Therapy Device (S250-FIT)Mevion Medical Systems, Inc.K243900eMotus Respiratory Motion Management SystemEmpnia, 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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