FDA 510(k) clearance · back to tracker

THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80

Fischer Imaging Corp. cleared K880522 on 1988-05-04, decision: substantially equivalent

K-number

K880522

Sponsor

Fischer Imaging Corp.

Device

THREE PHASE, DIAGNOSTIC X-RAY GENERATOR MICRO-X 80

Class

Class I

Decision

Substantially Equivalent

Decision date

1988-05-04

Product code

IZO

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1700

Official FDA record

Open K880522on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.