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FDA 510(k)

AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER

K-Number: K131786 · 2013-07-03

ApplicantAirstrip Technologies, LP
Decision Date2013-07-03
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER 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 2013-07-03 under 510(k) number K131786. 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 PHILIPS ADAPTER?

AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER is a medical device that received FDA 510(k) clearance on 2013-07-03. The listed applicant is Airstrip Technologies, LP. The 510(k) number is K131786.

When did AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER receive FDA 510(k) clearance?

AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER received FDA 510(k) clearance on 2013-07-03, under 510(k) number K131786.

Who is the listed applicant for AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER?

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 PHILIPS ADAPTER?

The FDA product code for AIRSTRIP REMOTE PATIENT MONITORING PHILIPS ADAPTER 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.

K122133AIRSTRIP 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)K100133AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1K090269AIRSTRIP 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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