Cleared Traditional

DOP 84

K810155 · Medlog GmbH Marketing Services · Radiology

May 1981

Decision

100d

Days

—

Risk

About This 510(k) Submission

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, 100 days after receiving the submission on January 21, 1981. This device falls under the Radiology review panel.

Submission Details

510(k) Number	K810155 FDA.gov
FDA Decision	Cleared SESE
Date Received	January 21, 1981
Decision Date	May 01, 1981
Days to Decision	100 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	—