510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800067Substantially Equivalent

Vita Lamp, Model 0350

Tensor Industries, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800067 is the FDA 510(k) clearance record for VITA LAMP, MODEL 0350, a class I device, cleared for Tensor Industries, Inc. on under FDA product code KZF (Device, Medical Examination, Ac Powered). FDA records list one 510(k) clearance for Tensor Industries, Inc. As of , FDA records show no recalls naming K800067.

Clearance record

Decision date
Received
(118 days to decision)
Product code
KZF Device, Medical Examination, Ac Powered
Regulation
21 CFR 880.6320
Device class
Class I
Review panel
General Hospital
Applicant
Tensor Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KZF

Trailing 12 months

FDA records hold no clearances under product code KZF in the trailing twelve months.

FDA records show no clearances under product code KZF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KZF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260