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FDA 510(k)

MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR

K-Number: K860025 · 1986-05-07

ApplicantMedicor USA , Ltd.
Decision Date1986-05-07
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1986-05-07 under 510(k) number K860025. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR?

MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR is a medical device that received FDA 510(k) clearance on 1986-05-07. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K860025.

When did MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR receive FDA 510(k) clearance?

MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR received FDA 510(k) clearance on 1986-05-07, under 510(k) number K860025.

Who is the listed applicant for MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR?

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

What is the FDA product code for MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR?

The FDA product code for MODEL MS-325 RADIOGRAPHIC X-RAY GENERATOR is KPR.

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Other records listing Medicor USA , Ltd. 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.

K861994MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEMK861995MODEL RS-3 RADIOGRAPHIC STANDK850761MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY CK851358MODEL BION 2/TYPE 90 ROOM IONIZERK851094MODEL BION 1/TYPE 1084T CAR IONIZERK843335FLOOR MOUNTED X-RAY TUBESTAND

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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