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FDA 510(k)

TECA TC2-64 TRANSCRANIAL DOPPLER

K-Number: K850137 · 1985-08-14

ApplicantTeca, Inc.
Decision Date1985-08-14
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TECA TC2-64 TRANSCRANIAL DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1985-08-14 under 510(k) number K850137. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA TC2-64 TRANSCRANIAL DOPPLER?

TECA TC2-64 TRANSCRANIAL DOPPLER is a medical device that received FDA 510(k) clearance on 1985-08-14. The listed applicant is Teca, Inc.. The 510(k) number is K850137.

When did TECA TC2-64 TRANSCRANIAL DOPPLER receive FDA 510(k) clearance?

TECA TC2-64 TRANSCRANIAL DOPPLER received FDA 510(k) clearance on 1985-08-14, under 510(k) number K850137.

Who is the listed applicant for TECA TC2-64 TRANSCRANIAL DOPPLER?

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 TC2-64 TRANSCRANIAL DOPPLER?

The FDA product code for TECA TC2-64 TRANSCRANIAL DOPPLER is DPW.

Related Clinical Trials

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.

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.

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Related Devices (Code: DPW)

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.

Official Source

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

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