AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING
K-Number: K122133 · 2012-10-02
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Device Summary
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 2012-10-02. The listed applicant is Airstrip Technologies, LP. The 510(k) number is K122133.
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 2012-10-02, under 510(k) number K122133.
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.
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
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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