Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K934941Substantially Equivalent

E-Z Temp II

Seven C'S, Inc., St. Louis MO / Traditional, Substantially Equivalent

K934941 is the FDA 510(k) clearance record for E-Z TEMP II, a class II device, cleared for Seven C'S, Inc. on under FDA product code KPD (Strip, Temperature, Forehead, Liquid Crystal). FDA records list one 510(k) clearance for Seven C'S, Inc. As of , FDA records show no recalls naming K934941.

Clearance record

Decision date
Received
(282 days to decision)
Product code
KPD Strip, Temperature, Forehead, Liquid Crystal
Regulation
21 CFR 880.2200
Device class
Class II
Review panel
General Hospital
Applicant
Seven C'S, Inc. P.O. Box 410494, St. Louis MO
510(k) summary
Statement
Third party review
No

Clearances, product code KPD

Trailing 12 months

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

FDA records show no clearances under product code KPD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPD, 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