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FDA 510(k)

TECA NEUROMAPPER 1620, BRAIN MAPPER

K-Number: K894088 · 1989-11-15

ApplicantTeca, Inc.
Decision Date1989-11-15
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TECA NEUROMAPPER 1620, BRAIN MAPPER is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1989-11-15 under 510(k) number K894088. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA NEUROMAPPER 1620, BRAIN MAPPER?

TECA NEUROMAPPER 1620, BRAIN MAPPER is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Teca, Inc.. The 510(k) number is K894088.

When did TECA NEUROMAPPER 1620, BRAIN MAPPER receive FDA 510(k) clearance?

TECA NEUROMAPPER 1620, BRAIN MAPPER received FDA 510(k) clearance on 1989-11-15, under 510(k) number K894088.

Who is the listed applicant for TECA NEUROMAPPER 1620, BRAIN MAPPER?

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 NEUROMAPPER 1620, BRAIN MAPPER?

The FDA product code for TECA NEUROMAPPER 1620, BRAIN MAPPER is OLT.

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Other records listing Teca, Inc. as applicant

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Related Devices (Code: OLT)

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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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