Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K922150Substantially Equivalent

Examination Lamp

Air-Shields, Inc., Hatboro PA / Traditional, Substantially Equivalent

K922150 is the FDA 510(k) clearance record for EXAMINATION LAMP, a class I device, cleared for Air-Shields, Inc. on under FDA product code KZF (Device, Medical Examination, Ac Powered). FDA records list 33 510(k) clearances for Air-Shields, Inc., from to . As of , FDA records show no recalls naming K922150.

Clearance record

Decision date
Received
(75 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
Air-Shields, Inc. 330 Jacksonville Rd., Hatboro PA
510(k) summary
Statement
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