Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VPW2877E7 X RAY POWER SUPPLY

K-Number: K905855 · 1991-02-13

ApplicantVarian Canada, Inc.
Decision Date1991-02-13
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VPW2877E7 X RAY POWER SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Varian Canada, Inc.. It received FDA 510(k) clearance on 1991-02-13 under 510(k) number K905855. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VPW2877E7 X RAY POWER SUPPLY?

VPW2877E7 X RAY POWER SUPPLY is a medical device that received FDA 510(k) clearance on 1991-02-13. The listed applicant is Varian Canada, Inc.. The 510(k) number is K905855.

When did VPW2877E7 X RAY POWER SUPPLY receive FDA 510(k) clearance?

VPW2877E7 X RAY POWER SUPPLY received FDA 510(k) clearance on 1991-02-13, under 510(k) number K905855.

Who is the listed applicant for VPW2877E7 X RAY POWER SUPPLY?

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

What is the FDA product code for VPW2877E7 X RAY POWER SUPPLY?

The FDA product code for VPW2877E7 X RAY POWER SUPPLY is IZO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Varian Canada, 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.

K953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORK923455HFG 350, 650, 1050K920938VJW2919 PNEUMATIC COMPRESSION UPGRADEK913234VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLYK910820VPW 2877E6 X-RAY POWER SUPPLYK904169VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY

View all 7 devices →

Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, 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.

↑