Generator, Biotec 876 Pulse

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K790031 ↗

Advisory committee

Unknown

FDA decision

SESP Substantially Equivalent — Postmarket Surveillance

• 700 Series Biomagnetometer

  Class II

  FDA 510(k) K901215 Active Cleared 25 Jun 1990

• Ibt Model Svi

  Class II

  FDA 510(k) K921821 Active Cleared 2 Nov 1992

• Magnes 2500 Wh Biomagnetometer

  Class II

  FDA 510(k) K962317 Active Cleared 7 May 1997

• Somatosensory Stimulus System

  Class II

  FDA 510(k) K913604 Active Cleared 9 Dec 1991

• Magnes II Biomagnetometer

  Class II

  FDA 510(k) K941553 Active Cleared 16 May 1996

• Biomagnetic Technologies Neuromagneometer

  Class II

  FDA 510(k) K854466 Active Cleared 4 Feb 1986

See all devices from Biomagnetic Technologies, Inc. →