510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K131023Substantially Equivalent

Theraflow Single Lumen and Theraflow Dual Lumen

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

K131023 is the FDA 510(k) clearance record for THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN, a class II device, cleared for Medical Products, LLC on under FDA product code NFB (Conserver, Oxygen). FDA records list 2 510(k) clearances for Medical Products, LLC, from to . As of , FDA records show no recalls naming K131023.

Clearance record

Decision date
Received
(182 days to decision)
Product code
NFB Conserver, Oxygen
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Medical Products, LLC 7437 Oaklandon Rd., Indianapolis IN
510(k) summary
Statement
Third party review
No

Clearances, product code NFB

Trailing 12 months

FDA records hold no clearances under product code NFB in the trailing twelve months.

FDA records show no clearances under product code NFB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NFB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260