510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802430Substantially Equivalent

Nebulizer, Medicinal

Dhd Medical Products Div. Diemolding Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802430 is the FDA 510(k) clearance record for NEBULIZER, MEDICINAL, a class I device, cleared for Dhd Medical Products Div. Diemolding Corp. on under FDA product code EPN (Pump, Nebulizer, Manual). FDA records list 43 510(k) clearances for Dhd Medical Products Div. Diemolding Corp., from to . As of , FDA records show no recalls naming K802430.

Clearance record

Decision date
Received
(17 days to decision)
Product code
EPN Pump, Nebulizer, Manual
Regulation
21 CFR 874.5220
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Dhd Medical Products Div. Diemolding Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EPN

Trailing 12 months

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

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