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510(k) K790031

GENERATOR, BIOTEC 876 PULSE by Biomagnetic Technologies, Inc.

K790031 is an FDA 510(k) premarket notification submitted by Biomagnetic Technologies, Inc. for the device "GENERATOR, BIOTEC 876 PULSE". The FDA issued a decision of SESP on January 2, 1979. Biomagnetic Technologies, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
January 2, 1979
Date Received
January 2, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Biomagnetic Technologies, Inc.

  • K993708 — BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG (December 3, 1999)
  • K962317 — MAGNES 2500 WH BIOMAGNETOMETER (May 7, 1997)
  • K941553 — MAGNES II BIOMAGNETOMETER (May 16, 1996)
  • K921821 — IBT MODEL SVI (November 2, 1992)
  • K913604 — SOMATOSENSORY STIMULUS SYSTEM (December 9, 1991)
  • K901215 — 700 SERIES BIOMAGNETOMETER (June 25, 1990)
  • K854466 — BIOMAGNETIC TECHNOLOGIES NEUROMAGNEOMETER (February 4, 1986)

FDA data resources