VITA LAMP, MODEL 0350— 510(k) K800067

Substantially Equivalent

Tensor Industries, Inc.

FDA 510(k) clearance K800067 for VITA LAMP, MODEL 0350, Substantially Equivalent on 1980-05-08. Applicant: Tensor Industries, Inc.. Device class: 1.

Clearance details

Applicant: Tensor Industries, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1980-01-11
Decision date: 1980-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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