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FDA 510(k)

HLIC NEEDLE-LESS VALVE

K-Number: K120548 · 2012-05-04

ApplicantHealth Line International Corporation
Decision Date2012-05-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HLIC NEEDLE-LESS VALVE 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 2012-05-04 under 510(k) number K120548. 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 HLIC NEEDLE-LESS VALVE?

HLIC NEEDLE-LESS VALVE is a medical device that received FDA 510(k) clearance on 2012-05-04. The listed applicant is Health Line International Corporation. The 510(k) number is K120548.

When did HLIC NEEDLE-LESS VALVE receive FDA 510(k) clearance?

HLIC NEEDLE-LESS VALVE received FDA 510(k) clearance on 2012-05-04, under 510(k) number K120548.

Who is the listed applicant for HLIC NEEDLE-LESS VALVE?

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 HLIC NEEDLE-LESS VALVE?

The FDA product code for HLIC NEEDLE-LESS VALVE is FPA.

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Other records listing Health Line International Corporation as applicant

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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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