Cleared Traditional

K828595 - MAXICAMERA 300A SMALL FIELD OF VIEW IMAGING SYSTEM (FDA 510(k) Clearance)

K828595 · General Electric Co. · Radiology device
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Dec 1982
Decision
49d
Days
-
Risk

K828595 is an FDA 510(k) clearance for the MAXICAMERA 300A SMALL FIELD OF VIEW IMAGING SYSTEM.

Submitted by General Electric Co. (Schenectady, US). The FDA issued a Cleared decision on December 14, 1982 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

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Submission Details

510(k) Number K828595 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 26, 1982
Decision Date December 14, 1982
Days to Decision 49 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 107d · This submission: 49d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -