510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K112702Substantially Equivalent

Imperial Surgical Ltd. Blankey and Solution Warning Cabinets

Imperial Surgical Ltd., Dundas, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112702 is the FDA 510(k) clearance record for IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS, a class II device, cleared for Imperial Surgical , Ltd. on under FDA product code LGZ (Warmer, Thermal, Infusion Fluid). FDA records list one 510(k) clearance for Imperial Surgical , Ltd. As of , FDA records show no recalls naming K112702.

Clearance record

Decision date
Received
(195 days to decision)
Product code
LGZ Warmer, Thermal, Infusion Fluid
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Imperial Surgical , Ltd. 4 Innovation Dr., Dundas, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LGZ

Trailing 12 months
3 clearances under product code LGZ in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LGZ, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260