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FDA 510(k)

IVAC NEEDLELESS INJECTION VALVE

K-Number: K922115 · 1993-10-12

ApplicantY
Decision Date1993-10-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC NEEDLELESS INJECTION VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K922115. 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 IVAC NEEDLELESS INJECTION VALVE?

IVAC NEEDLELESS INJECTION VALVE is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Y. The 510(k) number is K922115.

When did IVAC NEEDLELESS INJECTION VALVE receive FDA 510(k) clearance?

IVAC NEEDLELESS INJECTION VALVE received FDA 510(k) clearance on 1993-10-12, under 510(k) number K922115.

Who is the listed applicant for IVAC NEEDLELESS INJECTION VALVE?

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

What is the FDA product code for IVAC NEEDLELESS INJECTION VALVE?

The FDA product code for IVAC NEEDLELESS INJECTION VALVE 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 Y 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 78 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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