510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K904279Substantially Equivalent

Paroject Anesthetic Syringe

Ronvig Instruments, Ltd., Milford DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904279 is the FDA 510(k) clearance record for PAROJECT ANESTHETIC SYRINGE, a class II device, cleared for Ronvig Instruments, Ltd. on under FDA product code EGM (Injector, Jet, Mechanical-Powered). FDA records list 2 510(k) clearances for Ronvig Instruments, Ltd., from to . As of , FDA records show no recalls naming K904279.

Clearance record

Decision date
Received
(81 days to decision)
Product code
EGM Injector, Jet, Mechanical-Powered
Regulation
21 CFR 872.4475
Device class
Class II
Review panel
Dental
Applicant
Ronvig Instruments, Ltd. 18 Lexington Dr., Milford DE
Third party review
No

Clearances, product code EGM

Trailing 12 months

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

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