510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000482Substantially Equivalent

Modification to Autoject Mini

Owen Mumford Limited, Marietta GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000482 is the FDA 510(k) clearance record for MODIFICATION TO AUTOJECT MINI, a class II device, cleared for Owen Mumford, Ltd. on under FDA product code KZH (Introducer, Syringe Needle). FDA records list 13 510(k) clearances for Owen Mumford, Ltd., from to . As of , FDA records show no recalls naming K000482.

Clearance record

Decision date
Received
(21 days to decision)
Product code
KZH Introducer, Syringe Needle
Regulation
21 CFR 880.6920
Device class
Class II
Review panel
General Hospital
Applicant
Owen Mumford, Ltd. 849 Pickens Industrial Dr., Marietta GA
510(k) summary
Summary
Third party review
No

Clearances, product code KZH

Trailing 12 months

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

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