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FDA 510(k)

VITA LAMP, MODEL 0350

K-Number: K800067 · 1980-05-08

ApplicantTensor Industries, Inc.
Decision Date1980-05-08
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITA LAMP, MODEL 0350 is the device name listed in this FDA 510(k) record. The listed applicant is Tensor Industries, Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800067. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA LAMP, MODEL 0350?

VITA LAMP, MODEL 0350 is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Tensor Industries, Inc.. The 510(k) number is K800067.

When did VITA LAMP, MODEL 0350 receive FDA 510(k) clearance?

VITA LAMP, MODEL 0350 received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800067.

Who is the listed applicant for VITA LAMP, MODEL 0350?

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

What is the FDA product code for VITA LAMP, MODEL 0350?

The FDA product code for VITA LAMP, MODEL 0350 is KZF.

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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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