510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883848Substantially Equivalent for Some Indications

Kmi Oxy-Ban

Knight Medical, Inc., Houston TX / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K883848 is the FDA 510(k) clearance record for KMI OXY-BAN, a class II device, cleared for Knight Medical, Inc. on under FDA product code KPJ (Chamber, Oxygen, Topical, Extremity). FDA records list 5 510(k) clearances for Knight Medical, Inc., from to . As of , FDA records show no recalls naming K883848.

Clearance record

Decision date
Received
(171 days to decision)
Product code
KPJ Chamber, Oxygen, Topical, Extremity
Regulation
21 CFR 878.5650
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Knight Medical, Inc. 18120 Ammi Trl., Houston TX
Third party review
No

Clearances, product code KPJ

Trailing 12 months

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

FDA records show no clearances under product code KPJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPJ, 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