510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981509Substantially Equivalent

Tempo III

Medical Products, Inc., Chantilly VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981509 is the FDA 510(k) clearance record for TEMPO III, a class II device, cleared for Medical Products, Inc. on under FDA product code LGZ (Warmer, Thermal, Infusion Fluid). FDA records list 2 510(k) clearances for Medical Products, Inc., from to . As of , FDA records show no recalls naming K981509.

Clearance record

Decision date
Received
(73 days to decision)
Product code
LGZ Warmer, Thermal, Infusion Fluid
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Medical Products, Inc. 14014 Sullyfield Cir., #A, Chantilly VA
510(k) summary
Statement
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