MED-RX PATIENT DELIVERY SET
K-Number: K120375 · 2012-06-28
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Device Summary
Frequently Asked Questions
What is the MED-RX PATIENT DELIVERY SET?
MED-RX PATIENT DELIVERY SET is a medical device that received FDA 510(k) clearance on 2012-06-28. The listed applicant is Benlan, Inc.. The 510(k) number is K120375.
When did MED-RX PATIENT DELIVERY SET receive FDA 510(k) clearance?
MED-RX PATIENT DELIVERY SET received FDA 510(k) clearance on 2012-06-28, under 510(k) number K120375.
Who is the listed applicant for MED-RX PATIENT DELIVERY SET?
The FDA 510(k) record lists Benlan, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MED-RX PATIENT DELIVERY SET?
The FDA product code for MED-RX PATIENT DELIVERY SET is FPA.
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 Benlan, 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: FPA)
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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