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FDA 510(k)

TECA MF-20 MICROVASCULAR DOPPLER

K-Number: K850071 · 1985-04-02

ApplicantTeca, Inc.
Decision Date1985-04-02
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TECA MF-20 MICROVASCULAR 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 1985-04-02 under 510(k) number K850071. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA MF-20 MICROVASCULAR DOPPLER?

TECA MF-20 MICROVASCULAR DOPPLER is a medical device that received FDA 510(k) clearance on 1985-04-02. The listed applicant is Teca, Inc.. The 510(k) number is K850071.

When did TECA MF-20 MICROVASCULAR DOPPLER receive FDA 510(k) clearance?

TECA MF-20 MICROVASCULAR DOPPLER received FDA 510(k) clearance on 1985-04-02, under 510(k) number K850071.

Who is the listed applicant for TECA MF-20 MICROVASCULAR 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 MF-20 MICROVASCULAR DOPPLER?

The FDA product code for TECA MF-20 MICROVASCULAR DOPPLER is IYN.

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Related Devices (Code: IYN)

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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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