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FDA 510(k)

QFIX RADIOTHERAPY CHAIR

K-Number: K120916 · 2012-06-20

ApplicantWfr/Aquaplast Corp.
Decision Date2012-06-20
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QFIX RADIOTHERAPY CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Wfr/Aquaplast Corp.. It received FDA 510(k) clearance on 2012-06-20 under 510(k) number K120916. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QFIX RADIOTHERAPY CHAIR?

QFIX RADIOTHERAPY CHAIR is a medical device that received FDA 510(k) clearance on 2012-06-20. The listed applicant is Wfr/Aquaplast Corp.. The 510(k) number is K120916.

When did QFIX RADIOTHERAPY CHAIR receive FDA 510(k) clearance?

QFIX RADIOTHERAPY CHAIR received FDA 510(k) clearance on 2012-06-20, under 510(k) number K120916.

Who is the listed applicant for QFIX RADIOTHERAPY CHAIR?

The FDA 510(k) record lists Wfr/Aquaplast Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QFIX RADIOTHERAPY CHAIR?

The FDA product code for QFIX RADIOTHERAPY CHAIR is JAI.

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Other records listing Wfr/Aquaplast 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.

K060671KVUE IGRT TREATMENT TABLE TOP, RT-4551KV, KVUE INSERTS AND ACCESSORIES, VARIOUSK032156ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENTK021124ACCUFIX TILTING RADIOTRANSLUCENT HEADHOLDERK973370AQUAPLAST PALATAL STENTK943871AQUAPLAST TIE DOWN DRESSINGK942158AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS

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Related Devices (Code: JAI)

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.

K231612Eve Patient Positioner SystemLeo Cancer CareK182683Z-Robot Patient Positioning SystemChinan Biomedical Technology, Inc.K170502Patient Positioning SystemForte Automation Systems, Inc.K160518LEONI ORION SystemLeoni Cia Cable SystemK132084PROTURA COUCH SOFTWAREMed-Tec, Inc. D/B/A Civco Medical SolutionsK122413PATIENT POSITIONING SYSTEMForte Automation Systems, 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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