Cleared Traditional

K791852 - T-PC FOR R.F. M.D., M-501
(FDA 510(k) Clearance)

K791852 · Mem Medical, Inc. · Cardiovascular device
Oct 1979
Decision
12d
Days
—
Risk

K791852 is an FDA 510(k) clearance for the T-PC FOR R.F. M.D., M-501..

Submitted by Mem Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 1, 1979, 12 days after receiving the submission on September 19, 1979.

This device falls under the Cardiovascular FDA review panel.

Submission Details

510(k) Number K791852 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 1979
Decision Date October 01, 1979
Days to Decision 12 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary —

Device Classification

Product Code —
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