510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844202Substantially Equivalent

Moss Limb Load Monitor Lm101-1

Moss Rehabilation Hospital, Philadelphia PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844202 is the FDA 510(k) clearance record for MOSS LIMB LOAD MONITOR LM101-1, a class I device, cleared for Moss Rehabilation Hospital on under FDA product code IKE (Transducer, Miniature Pressure). FDA records list one 510(k) clearance for Moss Rehabilation Hospital. As of , FDA records show no recalls naming K844202.

Clearance record

Decision date
Received
(28 days to decision)
Product code
IKE Transducer, Miniature Pressure
Regulation
21 CFR 890.1615
Device class
Class I
Review panel
Physical Medicine
Applicant
Moss Rehabilation Hospital 12th. St. & Tabor Rd., Philadelphia PA
Third party review
No

Clearances, product code IKE

Trailing 12 months

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

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