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FDA 510(k)

MED-RX PATIENT DELIVERY SET

K-Number: K120375 · 2012-06-28

ApplicantBenlan, Inc.
Decision Date2012-06-28
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MED-RX PATIENT DELIVERY SET is the device name listed in this FDA 510(k) record. The listed applicant is Benlan, Inc.. It received FDA 510(k) clearance on 2012-06-28 under 510(k) number K120375. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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