Cleared Traditional

K133657 - DISCOVERY PET/CT 710 (FDA 510(k) Clearance)

Mar 2014
Decision
114d
Days
Class 2
Risk

K133657 is an FDA 510(k) clearance for the DISCOVERY PET/CT 710. This device is classified as a System, Tomography, Computed, Emission (Class II - Special Controls, product code KPS).

Submitted by Ge Medical Systems, LLC (Waukesha, US). The FDA issued a Cleared decision on March 21, 2014, 114 days after receiving the submission on November 27, 2013.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1200.

Submission Details

510(k) Number K133657 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 2013
Decision Date March 21, 2014
Days to Decision 114 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code KPS — System, Tomography, Computed, Emission
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.1200

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