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FDA 510(k)

TECA MODEL B9 ELECTROMYOGRAPH

K-Number: K781399 · 1978-09-20

ApplicantTeca, Inc.
Decision Date1978-09-20
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TECA MODEL B9 ELECTROMYOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781399. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA MODEL B9 ELECTROMYOGRAPH?

TECA MODEL B9 ELECTROMYOGRAPH is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Teca, Inc.. The 510(k) number is K781399.

When did TECA MODEL B9 ELECTROMYOGRAPH receive FDA 510(k) clearance?

TECA MODEL B9 ELECTROMYOGRAPH received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781399.

Who is the listed applicant for TECA MODEL B9 ELECTROMYOGRAPH?

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

What is the FDA product code for TECA MODEL B9 ELECTROMYOGRAPH?

The FDA product code for TECA MODEL B9 ELECTROMYOGRAPH is IKN.

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Other records listing Teca, 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.

K962283EEG ELECTRODESK903731SAPPHIRE SERIES 1P, 1L, 2L, AND 2MEK903004EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPHK896666P460, DG32 ELECTROENCEPHALOGRAPHK894889TECA NEUROMAPPER 386K894088TECA NEUROMAPPER 1620, BRAIN MAPPER

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Related Devices (Code: IKN)

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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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