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FDA 510(k)

TECNOTOMO

K-Number: K790132 · 1979-02-21

ApplicantTeknomed, Inc.
Decision Date1979-02-21
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TECNOTOMO is the device name listed in this FDA 510(k) record. The listed applicant is Teknomed, Inc.. It received FDA 510(k) clearance on 1979-02-21 under 510(k) number K790132. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNOTOMO?

TECNOTOMO is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Teknomed, Inc.. The 510(k) number is K790132.

When did TECNOTOMO receive FDA 510(k) clearance?

TECNOTOMO received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790132.

Who is the listed applicant for TECNOTOMO?

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

What is the FDA product code for TECNOTOMO?

The FDA product code for TECNOTOMO is IZF.

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Other records listing Teknomed, Inc. as applicant

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Related Devices (Code: IZF)

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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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