
Medcor, Inc.
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QUINTREX 0515 PROGRAMMABLE PULSE GEN. is an FDA 510(k)-cleared medical device (K802223) manufactured by Medcor, Inc.. This device is classified under the Unknown specialty. FDA clearance granted on September 11, 1980.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031