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FDA 510(k)

VJW2919 PNEUMATIC COMPRESSION UPGRADE

K-Number: K920938 · 1992-06-17

ApplicantVarian Canada, Inc.
Decision Date1992-06-17
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VJW2919 PNEUMATIC COMPRESSION UPGRADE 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 1992-06-17 under 510(k) number K920938. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VJW2919 PNEUMATIC COMPRESSION UPGRADE?

VJW2919 PNEUMATIC COMPRESSION UPGRADE is a medical device that received FDA 510(k) clearance on 1992-06-17. The listed applicant is Varian Canada, Inc.. The 510(k) number is K920938.

When did VJW2919 PNEUMATIC COMPRESSION UPGRADE receive FDA 510(k) clearance?

VJW2919 PNEUMATIC COMPRESSION UPGRADE received FDA 510(k) clearance on 1992-06-17, under 510(k) number K920938.

Who is the listed applicant for VJW2919 PNEUMATIC COMPRESSION UPGRADE?

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 VJW2919 PNEUMATIC COMPRESSION UPGRADE?

The FDA product code for VJW2919 PNEUMATIC COMPRESSION UPGRADE is IZH.

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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, 1050K913234VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLYK910820VPW 2877E6 X-RAY POWER SUPPLYK904169VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLYK905855VPW2877E7 X RAY POWER SUPPLY

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Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, 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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