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FDA 510(k)

VITALCARE I.V. ADMINISTRATION SET

K-Number: K050906 · 2005-08-23

Decision Date2005-08-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITALCARE I.V. ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Vitalcare Group, Inc.. It received FDA 510(k) clearance on 2005-08-23 under 510(k) number K050906. 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 VITALCARE I.V. ADMINISTRATION SET?

VITALCARE I.V. ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 2005-08-23. The listed applicant is Vitalcare Group, Inc.. The 510(k) number is K050906.

When did VITALCARE I.V. ADMINISTRATION SET receive FDA 510(k) clearance?

VITALCARE I.V. ADMINISTRATION SET received FDA 510(k) clearance on 2005-08-23, under 510(k) number K050906.

Who is the listed applicant for VITALCARE I.V. ADMINISTRATION SET?

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

What is the FDA product code for VITALCARE I.V. ADMINISTRATION SET?

The FDA product code for VITALCARE I.V. ADMINISTRATION 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 Vitalcare Group, 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 8 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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