510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K203168Substantially Equivalent

LifeLens Wireless ECG Monitor

LifeLens Technologies, Inc., Warminster PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203168 is the FDA 510(k) clearance record for LifeLens Wireless ECG Monitor, a class II device, cleared for LifeLens Technologies, Inc. on under FDA product code DSH (Recorder, Magnetic Tape, Medical). FDA records list 2 510(k) clearances for LifeLens Technologies, Inc., from to . As of , FDA records show no recalls naming K203168.

Clearance record

Decision date
Received
(270 days to decision)
Product code
DSH Recorder, Magnetic Tape, Medical
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
LifeLens Technologies, Inc. 1 Ivybrook Blvd., Suite 115, Warminster PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DSH

Trailing 12 months
3 clearances under product code DSH in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260