510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902255Substantially Equivalent

Omron Pulse Stimulator Model Hv-F05

Omron Electronics, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902255 is the FDA 510(k) clearance record for OMRON PULSE STIMULATOR MODEL HV-F05, a class II device, cleared for Omron Electronics, Inc. on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 10 510(k) clearances for Omron Electronics, Inc., from to . As of , FDA records show no recalls naming K902255.

Clearance record

Decision date
Received
(163 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Omron Electronics, Inc. 1615 L St., NW, Washington DC
Third party review
No

Clearances, product code IPF

Trailing 12 months
3 clearances under product code IPF in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IPF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20262
July 20260
August 20260
September 20260
October 20260