Edentec Digital Charter Model 3710

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K910871 ↗

FDA Product Code

DSF

Device Class

Class I

Regulation

21 CFR Part 870.2810

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Edentrace Airflow 3171/Sleep Lab Airflow 3170

  Class II

  FDA 510(k) K913749 Active Cleared 2 Jul 1992

• Model 2000W Option H Configuration

  Class II

  FDA 510(k) K871302 Active Cleared 20 Apr 1987

• Edentrace Multi-Charter Model 3700

  Class I

  FDA 510(k) K883315 Active Cleared 28 Dec 1988

• Edentec Model 2001 Modular Memory Unit (Mmu)

  Class II

  FDA 510(k) K892227 Active Cleared 20 Jun 1989

• Edentec Model 2860 Pressure Meter

  Class II

  FDA 510(k) K891540 Active Cleared 1 Jun 1989

• Edentrace 670 System Multichannel Recorder W/Oxim.

  Class I

  FDA 510(k) K893561 Active Cleared 25 Aug 1989

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