Edentec Model 2860 Pressure Meter

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

510(k) Number

K891540 ↗

FDA Product Code

BYE

Device Class

Class II

Regulation

21 CFR Part 868.5965

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K913749 Active Cleared 2 Jul 1992

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  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

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  Class I

  FDA 510(k) K893561 Active Cleared 25 Aug 1989

• Edentec Model 3711 Digital Recorder

  Class II

  FDA 510(k) K910870 Active Cleared 29 Aug 1991

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