510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K073363Substantially Equivalent

Thermostat 900 Administration Set, Model Ash 100, 200 and 300

Paladin Biomedical Corporation, Weston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073363 is the FDA 510(k) clearance record for THERMOSTAT 900 ADMINISTRATION SET, MODEL ASH 100, 200 AND 300, a class II device, cleared for Paladin Biomedical Corporation on under FDA product code LGZ (Warmer, Thermal, Infusion Fluid). FDA records list one 510(k) clearance for Paladin Biomedical Corporation. As of , FDA records show no recalls naming K073363.

Clearance record

Decision date
Received
(111 days to decision)
Product code
LGZ Warmer, Thermal, Infusion Fluid
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Paladin Biomedical Corporation 506 Boston Post Rd., Weston MA
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