Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K780757Substantially Equivalent

Kryorack/4

Streck Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent

K780757 is the FDA 510(k) clearance record for KRYORACK/4, a class I device, cleared for Streck Laboratories, Inc. on under FDA product code JRR (Regulator, Temperature). FDA records list 70 510(k) clearances for Streck Laboratories, Inc., from to . As of , FDA records show no recalls naming K780757.

Clearance record

Decision date
Received
(29 days to decision)
Product code
JRR Regulator, Temperature
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Streck Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JRR

Trailing 12 months

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

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