Edentec Corp.
Edentec Corp. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1996.
Top product codes for Edentec Corp.
Recent clearances by Edentec Corp.
- K953363 — OXIFLOW DIGITAL RECORDER
- K953540 — EEE
- K921819 — EDENTEC MODEL 3710 I DIGITAL PRINTER
- K913749 — EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170
- K910870 — EDENTEC MODEL 3711 DIGITAL RECORDER
- K910871 — EDENTEC DIGITAL CHARTER MODEL 3710
- K905575 — MODIFIED MODELS 2000W AND 2000W OPTION H APNEA MON
- K901060 — EDENTEC MODEL 2000W SYSTEM 700 MONITOR
- K893561 — EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM.
- K892227 — EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU)
- K891540 — EDENTEC MODEL 2860 PRESSURE METER
- K884614 — EDENTEC MODEL 2000W OPTION S CARDIO-RESP. PROCESS.
- K884388 — EDENTEC MODEL 4700 SCANNER
- K883315 — EDENTRACE MULTI-CHARTER MODEL 3700
- K881820 — EDENTEC MODEL 2800/2801 OXIMETER/PULSE OXIMETER
- K873081 — EDENTEC MULTI-CHANNEL RECORDER
- K871302 — MODEL 2000W OPTION H CONFIGURATION
- K844327 — EDENTEC MODEL 2000W APNEA MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.