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FDA 510(k)

AIRSTRIP RPM FOR LIFENET CONSULT

K-Number: K121712 · 2012-11-20

ApplicantAirstrip Technologies, Inc.
Decision Date2012-11-20
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AIRSTRIP RPM FOR LIFENET CONSULT is the device name listed in this FDA 510(k) record. The listed applicant is Airstrip Technologies, Inc.. It received FDA 510(k) clearance on 2012-11-20 under 510(k) number K121712. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRSTRIP RPM FOR LIFENET CONSULT?

AIRSTRIP RPM FOR LIFENET CONSULT is a medical device that received FDA 510(k) clearance on 2012-11-20. The listed applicant is Airstrip Technologies, Inc.. The 510(k) number is K121712.

When did AIRSTRIP RPM FOR LIFENET CONSULT receive FDA 510(k) clearance?

AIRSTRIP RPM FOR LIFENET CONSULT received FDA 510(k) clearance on 2012-11-20, under 510(k) number K121712.

Who is the listed applicant for AIRSTRIP RPM FOR LIFENET CONSULT?

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

What is the FDA product code for AIRSTRIP RPM FOR LIFENET CONSULT?

The FDA product code for AIRSTRIP RPM FOR LIFENET CONSULT is MSX.

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Other records listing Airstrip Technologies, Inc. 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.

K211949AirStrip ONE Web Client with Alarm Communication Management (ACM)K182226AirStrip RPM InvisionHeart AdapterK160862AirStrip RPM

Related Devices (Code: MSX)

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.

K261287Digistat CareAscom Ums Srl UnipersonaleK260211Dashboard (P007000)Hill-Rom, Inc.K261367Corsano CardioWatch 287-2 SystemCorsano Health B.V.K253654IntelliVue Measurement Rack 6000 (867317)Philips Medizin Systeme Böblingen GmbHK243270TigerConnect Alarm ManagementTigerconnectK242728BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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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