510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800667Substantially Equivalent

Monitemp Blood Pack Temp. Monitor

Liquid Crystal Products, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800667 is the FDA 510(k) clearance record for MONITEMP BLOOD PACK TEMP. MONITOR, a class II device, cleared for Liquid Crystal Products, Inc. on under FDA product code KSE (Refrigerator, Freezer, Blood Storage). FDA records list 3 510(k) clearances for Liquid Crystal Products, Inc., from to . As of , FDA records show no recalls naming K800667.

Clearance record

Decision date
Received
(21 days to decision)
Product code
KSE Refrigerator, Freezer, Blood Storage
Regulation
21 CFR 864.9700
Device class
Class II
Review panel
Hematology
Applicant
Liquid Crystal Products, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KSE

Trailing 12 months

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

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