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FDA 510(k)

MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900

K-Number: K040385 · 2004-04-07

ApplicantQuest Medical, Inc.
Decision Date2004-04-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900 is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 2004-04-07 under 510(k) number K040385. 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 MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900?

MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900 is a medical device that received FDA 510(k) clearance on 2004-04-07. The listed applicant is Quest Medical, Inc.. The 510(k) number is K040385.

When did MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900 receive FDA 510(k) clearance?

MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900 received FDA 510(k) clearance on 2004-04-07, under 510(k) number K040385.

Who is the listed applicant for MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900?

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

What is the FDA product code for MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900?

The FDA product code for MULTIPORT MANIFOLD SET WITH SWABABLE VALVES, MODEL 9900 is FPA.

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Related Devices (Code: FPA)

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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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