Telectronics, Inc.

Telectronics, Inc. holds 107 FDA 510(k) medical device clearances, first cleared 1977, most recent 1990.

Clearances by Telectronics, Inc. — page 2

101–107 of 107

K772334 — MONITOR, CARDIAC, W/BLOOD PRESS.&TEMPCode DSK·1978-02-21
K772332 — MONITOR, CARDIAC, BEDSIDECode DRT·1978-02-13
K772333 — RECORDER, PAPER, ECGCode DSF·1978-02-13
K780113 — CARDIAC PULSE GENERATOR, MODEL 160BCode DXY·1978-02-13
K772331 — RESTERIL. OF IMPLANT. ELECT. & ADAPTERCode DTB·1978-01-11
K772026 — CARDIAC PULSE GENERATOR, MODEL 150LCode DXY·1977-11-03
K771670 — IMPLANTED PACEMAKER PLUSE GENERATORCode DXY·1977-09-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.