510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K853849Substantially Equivalent

Medar Apm Force Transducer

Medar Corp., Inc., Scarsdale NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853849 is the FDA 510(k) clearance record for MEDAR APM FORCE TRANSDUCER, a class II device, cleared for Medar Corp., Inc. on under FDA product code BXN (Stimulator, Nerve, Battery-Powered). FDA records list one 510(k) clearance for Medar Corp., Inc. As of , FDA records show no recalls naming K853849.

Clearance record

Decision date
Received
(109 days to decision)
Product code
BXN Stimulator, Nerve, Battery-Powered
Regulation
21 CFR 868.2775
Device class
Class II
Review panel
Anesthesiology
Applicant
Medar Corp., Inc. P.O. Box N-H, Scarsdale NY
Third party review
No

Clearances, product code BXN

Trailing 12 months

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

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