510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K872525Substantially Equivalent

A.l.a.r.m. (Adjust. Leg & Ankle Repositioning Mech

M.C. Johnson Co., Inc., Leominster MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872525 is the FDA 510(k) clearance record for A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH, a class II device, cleared for M.C. Johnson Co., Inc. on under FDA product code KPR (System, X-Ray, Stationary). FDA records list 3 510(k) clearances for M.C. Johnson Co., Inc., from to . As of , FDA records show no recalls naming K872525.

Clearance record

Decision date
Received
(242 days to decision)
Product code
KPR System, X-Ray, Stationary
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
M.C. Johnson Co., Inc. 758 Main St., Leominster MA
Third party review
No

Clearances, product code KPR

Trailing 12 months
7 clearances under product code KPR in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KPR, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20262
September 20261
October 20260