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FDA 510(k)

DESERET(R) I.V. LOOP AND DESERET (R) J LOOP

K-Number: K950303 · 1995-03-14

ApplicantBecton Dickinson Vascular Access, Inc.
Decision Date1995-03-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET(R) I.V. LOOP AND DESERET (R) J LOOP is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vascular Access, Inc.. It received FDA 510(k) clearance on 1995-03-14 under 510(k) number K950303. 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 DESERET(R) I.V. LOOP AND DESERET (R) J LOOP?

DESERET(R) I.V. LOOP AND DESERET (R) J LOOP is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K950303.

When did DESERET(R) I.V. LOOP AND DESERET (R) J LOOP receive FDA 510(k) clearance?

DESERET(R) I.V. LOOP AND DESERET (R) J LOOP received FDA 510(k) clearance on 1995-03-14, under 510(k) number K950303.

Who is the listed applicant for DESERET(R) I.V. LOOP AND DESERET (R) J LOOP?

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

What is the FDA product code for DESERET(R) I.V. LOOP AND DESERET (R) J LOOP?

The FDA product code for DESERET(R) I.V. LOOP AND DESERET (R) J LOOP is FPA.

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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.

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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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