Cleared Traditional

GENERATOR, BIOTEC 876 PULSE

K790031 · Biomagnetic Technologies, Inc. · Cardiovascular

Jan 1979

Decision

—

Days

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Risk

About This 510(k) Submission

K790031 is an FDA 510(k) clearance for the GENERATOR, BIOTEC 876 PULSE, submitted by Biomagnetic Technologies, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 2, 1979. This device falls under the Cardiovascular review panel.

Submission Details

510(k) Number	K790031 FDA.gov
FDA Decision	Cleared SESP
Date Received	January 02, 1979
Decision Date	January 02, 1979
Days to Decision	—
Submission Type	Traditional
Review Panel	Cardiovascular (CV)
Summary	—