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FDA 510(k)

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1

K-Number: K100133 · 2010-07-23

ApplicantAirstrip Technologies, LP
Decision Date2010-07-23
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 is the device name listed in this FDA 510(k) record. The listed applicant is Airstrip Technologies, LP. It received FDA 510(k) clearance on 2010-07-23 under 510(k) number K100133. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1?

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 is a medical device that received FDA 510(k) clearance on 2010-07-23. The listed applicant is Airstrip Technologies, LP. The 510(k) number is K100133.

When did AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 receive FDA 510(k) clearance?

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 received FDA 510(k) clearance on 2010-07-23, under 510(k) number K100133.

Who is the listed applicant for AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1?

The FDA 510(k) record lists Airstrip Technologies, LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1?

The FDA product code for AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 is MWI.

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Other records listing Airstrip Technologies, LP as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K131786AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTERK122133AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWINGK121871AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWINGK112235AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWINGK110503AIRSTRIP REMOTE PATIENT MONITORING (RPM)K090269AIRSTRIP OB

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Related Devices (Code: MWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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