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FDA 510(k)

GENERATOR, BIOTEC 876 PULSE

K-Number: K790031 · 1979-01-02

ApplicantBiomagnetic Technologies, Inc.
Decision Date1979-01-02
Product Code
DecisionUnknown

Device Summary

GENERATOR, BIOTEC 876 PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Biomagnetic Technologies, Inc.. It received FDA 510(k) clearance on 1979-01-02 under 510(k) number K790031. FDA Decision: Unknown.

Frequently Asked Questions

What is the GENERATOR, BIOTEC 876 PULSE?

GENERATOR, BIOTEC 876 PULSE is a medical device that received FDA 510(k) clearance on 1979-01-02. The listed applicant is Biomagnetic Technologies, Inc.. The 510(k) number is K790031.

When did GENERATOR, BIOTEC 876 PULSE receive FDA 510(k) clearance?

GENERATOR, BIOTEC 876 PULSE received FDA 510(k) clearance on 1979-01-02, under 510(k) number K790031.

Who is the listed applicant for GENERATOR, BIOTEC 876 PULSE?

The FDA 510(k) record lists Biomagnetic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Biomagnetic Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K993708BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEGK962317MAGNES 2500 WH BIOMAGNETOMETERK941553MAGNES II BIOMAGNETOMETERK921821IBT MODEL SVIK913604SOMATOSENSORY STIMULUS SYSTEMK901215700 SERIES BIOMAGNETOMETER

View all 8 devices →

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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