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FDA 510(k)

G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN

K-Number: K902985 · 1990-12-19

ApplicantElectromek Diagnostic Systems, Inc.
Decision Date1990-12-19
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN is the device name listed in this FDA 510(k) record. The listed applicant is Electromek Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1990-12-19 under 510(k) number K902985. 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 G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN?

G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN is a medical device that received FDA 510(k) clearance on 1990-12-19. The listed applicant is Electromek Diagnostic Systems, Inc.. The 510(k) number is K902985.

When did G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN receive FDA 510(k) clearance?

G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN received FDA 510(k) clearance on 1990-12-19, under 510(k) number K902985.

Who is the listed applicant for G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN?

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

What is the FDA product code for G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN?

The FDA product code for G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN 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.

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Other records listing Electromek Diagnostic Systems, 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.

K902986G.E. DXD 325/350/350II/DXD 525/525II GENERATORSK902987G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORSK902988G.E. MSI 850/850II/1250 THREE PHASE GENERATORSK902982G.E. POLARIX II C-ARMK902981G.E. FLUOROCON 300 IMAGING SYSTEMK902983SIEMEN'S SIREMOBILE II C-ARM

View all 11 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.

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