510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K905151Substantially Equivalent

Vancomycin Disk-5 Mcg

Remel Inc, Lenexa KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905151 is the FDA 510(k) clearance record for VANCOMYCIN DISK-5 MCG, a class I device, cleared for Remel Co. on under FDA product code JTO (Discs, Strips And Reagents, Microorganism Differentiation). FDA records list 107 510(k) clearances for Remel Co., from to . As of , FDA records show no recalls naming K905151.

Clearance record

Decision date
Received
(71 days to decision)
Product code
JTO Discs, Strips And Reagents, Microorganism Differentiation
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Remel Co. 12076 Santa Fe Dr., Lenexa KS
Third party review
No

Clearances, product code JTO

Trailing 12 months

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

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