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FDA 510(k)

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING

K-Number: K112235 · 2011-08-26

Decision Date2011-08-26
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING 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 2011-08-26 under 510(k) number K112235. 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?

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING is a medical device that received FDA 510(k) clearance on 2011-08-26. The listed applicant is Airstrip Technologies, LP. The 510(k) number is K112235.

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

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING received FDA 510(k) clearance on 2011-08-26, under 510(k) number K112235.

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

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?

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

Related Clinical Trials

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.

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.

View all 8 devices →

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.

Official Source

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

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