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FDA 510(k)

PRESSURE STOPCOCK/MANIFOLD

K-Number: K960431 · 1996-10-29

ApplicantScientific Device Manufacturer, LLC
Decision Date1996-10-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRESSURE STOPCOCK/MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Device Manufacturer, LLC. It received FDA 510(k) clearance on 1996-10-29 under 510(k) number K960431. 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 PRESSURE STOPCOCK/MANIFOLD?

PRESSURE STOPCOCK/MANIFOLD is a medical device that received FDA 510(k) clearance on 1996-10-29. The listed applicant is Scientific Device Manufacturer, LLC. The 510(k) number is K960431.

When did PRESSURE STOPCOCK/MANIFOLD receive FDA 510(k) clearance?

PRESSURE STOPCOCK/MANIFOLD received FDA 510(k) clearance on 1996-10-29, under 510(k) number K960431.

Who is the listed applicant for PRESSURE STOPCOCK/MANIFOLD?

The FDA 510(k) record lists Scientific Device Manufacturer, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE STOPCOCK/MANIFOLD?

The FDA product code for PRESSURE STOPCOCK/MANIFOLD is FPA.

Related Clinical Trials

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Other records listing Scientific Device Manufacturer, LLC 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.

K960764SAFE-CATHK961290IUP - TIP TRANS, IUP - PROXI TRANSK960430CONTROL SYRINGEK960917PERCUGLIDEK952579TOCO TRANSDUCER

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

Official Source

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