Cleared Traditional

K810155 - DOP 84 (FDA 510(k) Clearance)

K810155 · Medlog GmbH Marketing Services · Radiology device
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May 1981
Decision
100d
Days
-
Risk

K810155 is an FDA 510(k) clearance for the DOP 84.

Submitted by Medlog GmbH Marketing Services (Mchenry, US). The FDA issued a Cleared decision on May 1, 1981 after a review of 100 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K810155 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 21, 1981
Decision Date May 01, 1981
Days to Decision 100 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
7d faster than avg
Panel avg: 107d · This submission: 100d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -