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FDA 510(k)

INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)

K-Number: K952160 · 1995-09-21

ApplicantMedex, Inc.
Decision Date1995-09-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1995-09-21 under 510(k) number K952160. 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 INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)?

INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) is a medical device that received FDA 510(k) clearance on 1995-09-21. The listed applicant is Medex, Inc.. The 510(k) number is K952160.

When did INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) receive FDA 510(k) clearance?

INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) received FDA 510(k) clearance on 1995-09-21, under 510(k) number K952160.

Who is the listed applicant for INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)?

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

What is the FDA product code for INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA)?

The FDA product code for INTRAVASCULAR (I-V) ADMININISTRATION SET (DVGENPERS FPA) 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 Medex, 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.

View all 48 devices →

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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