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FDA 510(k)

VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY

K-Number: K904169 · 1991-02-19

ApplicantVarian Canada, Inc.
Decision Date1991-02-19
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY 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 1991-02-19 under 510(k) number K904169. 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 VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY?

VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Varian Canada, Inc.. The 510(k) number is K904169.

When did VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY receive FDA 510(k) clearance?

VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY received FDA 510(k) clearance on 1991-02-19, under 510(k) number K904169.

Who is the listed applicant for VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY 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 VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY?

The FDA product code for VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY is IZO.

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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 SUPPLYK905855VPW2877E7 X RAY POWER SUPPLY

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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.

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