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FDA 510(k)

HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS

K-Number: K060352 · 2006-05-31

Decision Date2006-05-31
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS is the device name listed in this FDA 510(k) record. The listed applicant is Health Line International Corporation. It received FDA 510(k) clearance on 2006-05-31 under 510(k) number K060352. 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 HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS?

HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS is a medical device that received FDA 510(k) clearance on 2006-05-31. The listed applicant is Health Line International Corporation. The 510(k) number is K060352.

When did HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS receive FDA 510(k) clearance?

HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS received FDA 510(k) clearance on 2006-05-31, under 510(k) number K060352.

Who is the listed applicant for HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS?

The FDA 510(k) record lists Health Line International Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS?

The FDA product code for HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS 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 Health Line International Corporation 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 10 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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