Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K060851Substantially Equivalent

Soft Sack IV Fluid Warmer, the Floormount IV Fluid Warmer, the Pak 2 IV Warmer and the Thermal Sac Pressure Infuser

Smithworks, Inc., Bellevue WA / Traditional, Substantially Equivalent

K060851 is the FDA 510(k) clearance record for SOFT SACK IV FLUID WARMER, THE FLOORMOUNT IV FLUID WARMER, THE PAK 2 IV WARMER AND THE THERMAL SAC PRESSURE INFUSER, a class II device, cleared for The Smithworks Company on under FDA product code LGZ (Warmer, Thermal, Infusion Fluid). FDA records list one 510(k) clearance for The Smithworks Company. As of , FDA records show no recalls naming K060851.

Clearance record

Decision date
Received
(269 days to decision)
Product code
LGZ Warmer, Thermal, Infusion Fluid
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
The Smithworks Company 2615 102nd Ave. NE, Bellevue WA
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