Home / 510(k) Clearances / K910870

510(k) K910870

EDENTEC MODEL 3711 DIGITAL RECORDER by Edentec Corp. — Product Code DRT

K910870 is an FDA 510(k) premarket notification submitted by Edentec Corp. for the device "EDENTEC MODEL 3711 DIGITAL RECORDER". The FDA issued a decision of Substantially Equivalent on August 29, 1991. The device falls under product code DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)), a Class II device regulated under 21 CFR 870.2300. Edentec Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1991
Date Received
March 1, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type

Other clearances by Edentec Corp.

  • K953363 — OXIFLOW DIGITAL RECORDER (February 6, 1996)
  • K953540 — EEE (August 25, 1995)
  • K921819 — EDENTEC MODEL 3710 I DIGITAL PRINTER (October 22, 1993)
  • K913749 — EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 (July 2, 1992)
  • K910871 — EDENTEC DIGITAL CHARTER MODEL 3710 (August 29, 1991)
  • K905575 — MODIFIED MODELS 2000W AND 2000W OPTION H APNEA MON (June 20, 1991)
  • K901060 — EDENTEC MODEL 2000W SYSTEM 700 MONITOR (May 15, 1990)
  • K893561 — EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM. (August 25, 1989)
  • K892227 — EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU) (June 20, 1989)
  • K891540 — EDENTEC MODEL 2860 PRESSURE METER (June 1, 1989)

Other clearances for product code DRT

  • K261286 — The Circadia C300 System (C300) (May 20, 2026)
  • K252676 — The Circadia C300 System (C300) (February 3, 2026)
  • K253388 — Sleepiz One+ (Model 2.5) (January 28, 2026)
  • K251364 — Sleepiz One+ (2.5) (July 29, 2025)
  • K234003 — The Circadia C200 System (May 30, 2024)
  • K232354 — Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central (March 22, 2024)
  • K231733 — Neteera 130H-Plus Vital Sign Monitoring Sensor (February 9, 2024)
  • K223163 — Sleepiz One+ (August 18, 2023)
  • K212143 — Neteera 130H/131H Vital Sign Monitoring Sensor (September 28, 2022)
  • K202138 — Cardiac Trigger Monitor (May 14, 2021)

FDA data resources