MEDSTAR 150
K-Number: K013081 · 2001-11-20
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Device Summary
Frequently Asked Questions
What is the MEDSTAR 150?
MEDSTAR 150 is a medical device that received FDA 510(k) clearance on 2001-11-20. The listed applicant is Mednet Services, Inc.. The 510(k) number is K013081.
When did MEDSTAR 150 receive FDA 510(k) clearance?
MEDSTAR 150 received FDA 510(k) clearance on 2001-11-20, under 510(k) number K013081.
Who is the listed applicant for MEDSTAR 150?
The FDA 510(k) record lists Mednet Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDSTAR 150?
The FDA product code for MEDSTAR 150 is IPF.
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 Mednet Services, 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.
Related Devices (Code: IPF)
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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