510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K895671Substantially Equivalent

Stimtrac II Catalog Number 78-8500

Stimtech Products, Southbridge MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895671 is the FDA 510(k) clearance record for STIMTRAC II CATALOG NUMBER 78-8500, a class II device, cleared for Stimtech Products on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 3 510(k) clearances for Stimtech Products, from to . As of , FDA records show no recalls naming K895671.

Clearance record

Decision date
Received
(47 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Stimtech Products East Main St., Southbridge MA
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