510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110503Substantially Equivalent

Airstrip Remote Patient Monitoring (Rpm)

AirStrip Technologies, Inc., San Antonio TX / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K110503 is the FDA 510(k) clearance record for AIRSTRIP REMOTE PATIENT MONITORING (RPM), a class II device, cleared for Airstrip Technologies, LP on under FDA product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)). FDA records list 15 510(k) clearances for Airstrip Technologies, LP, from to . As of , FDA records show no recalls naming K110503.

Clearance record

Decision date
Received
(16 days to decision)
Product code
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Regulation
21 CFR 870.2300
Device class
Class II
Review panel
Cardiovascular
Applicant
Airstrip Technologies, LP 3303 Oakwell Ct., Suite 200, San Antonio TX
510(k) summary
Statement
Third party review
Yes

Clearances, product code MWI

Trailing 12 months
5 clearances under product code MWI 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 MWI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20262
September 20260
October 20260