510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K991888Substantially Equivalent

Miniject

Spartan Ultrasonics, Inc., Fenton MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K991888 is the FDA 510(k) clearance record for MINIJECT, a class II device, cleared for Spartan Ultrasonics, Inc. on under FDA product code EJI (Syringe, Cartridge). FDA records list 2 510(k) clearances for Spartan Ultrasonics, Inc., from to . As of , FDA records show no recalls naming K991888.

Clearance record

Decision date
Received
(84 days to decision)
Product code
EJI Syringe, Cartridge
Regulation
21 CFR 872.6770
Device class
Class II
Review panel
Dental
Applicant
Spartan Ultrasonics, Inc. 1663 Fenton Business Park Ct., Fenton MO
510(k) summary
Summary
Third party review
No

Clearances, product code EJI

Trailing 12 months

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

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