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FDA 510(k)

MULTI PULSE POWER UNIT GENERATOR

K-Number: K892943 · 1989-05-22

ApplicantGE Medical Systems
Decision Date1989-05-22
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI PULSE POWER UNIT GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1989-05-22 under 510(k) number K892943. 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 MULTI PULSE POWER UNIT GENERATOR?

MULTI PULSE POWER UNIT GENERATOR is a medical device that received FDA 510(k) clearance on 1989-05-22. The listed applicant is GE Medical Systems. The 510(k) number is K892943.

When did MULTI PULSE POWER UNIT GENERATOR receive FDA 510(k) clearance?

MULTI PULSE POWER UNIT GENERATOR received FDA 510(k) clearance on 1989-05-22, under 510(k) number K892943.

Who is the listed applicant for MULTI PULSE POWER UNIT GENERATOR?

The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI PULSE POWER UNIT GENERATOR?

The FDA product code for MULTI PULSE POWER UNIT GENERATOR is IZO.

Related Clinical Trials

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Other records listing GE Medical Systems 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.

K253808AIR Recon DLK220848Venue FitK220851VenueK173341Vivid E80, Vivid E90, Vivid E95K103411IDEAL IQ SOFTWARE OPTIONK073138CARDIQ EXPRESS VERSION 2.0

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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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