510(k) Report

FDA applicant

Liquid Crystal Products, Inc.

Walker, MI3 decisions1980–19820 recalls

FDA records 3 decisions for Liquid Crystal Products, Inc. (Walker, MI) from 1980 to 1982: 3 510(k) clearances. Most are in product codes KSE (Refrigerator, Freezer, Blood Storage) and KPP (Peritoneal Dialysate Filter). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, hematology panel, where it files most

How often FDA has decided Liquid Crystal Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Liquid Crystal Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Liquid Crystal Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KSERefrigerator, Freezer, Blood Storage1decision
  • KPPPeritoneal Dialysate Filter1decision
  • KPDStrip, Temperature, Forehead, Liquid Crystal1decision

What has FDA decided for it lately?

  • K821312Temptrend Temperature Trend IndicatorLiquid Crystal Products, Inc. · 1982
  • K800666Quik-TempLiquid Crystal Products, Inc. · 1980
  • K800667Monitemp Blood Pack Temp. MonitorLiquid Crystal Products, Inc. · 1980

All 3 as Liquid Crystal Products, Inc. →

Other applicant names beginning “Liquid”

FDA records each applicant name separately; these may or may not be the same firm.

Liquid Carbonic Corp. 5Liquid Technology Corp. 3Liquid Air Corp. 2Liquid Crystal Sciences, Inc. 1Liquid Carbonic Industrial Gases 1