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FDA 510(k)

S.C.T. MULTI PORT, INJECTION SITE

K-Number: K864296 · 1987-03-02

ApplicantSalt Creek Medical Technologies
Decision Date1987-03-02
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

S.C.T. MULTI PORT, INJECTION SITE is the device name listed in this FDA 510(k) record. The listed applicant is Salt Creek Medical Technologies. It received FDA 510(k) clearance on 1987-03-02 under 510(k) number K864296. 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 S.C.T. MULTI PORT, INJECTION SITE?

S.C.T. MULTI PORT, INJECTION SITE is a medical device that received FDA 510(k) clearance on 1987-03-02. The listed applicant is Salt Creek Medical Technologies. The 510(k) number is K864296.

When did S.C.T. MULTI PORT, INJECTION SITE receive FDA 510(k) clearance?

S.C.T. MULTI PORT, INJECTION SITE received FDA 510(k) clearance on 1987-03-02, under 510(k) number K864296.

Who is the listed applicant for S.C.T. MULTI PORT, INJECTION SITE?

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

What is the FDA product code for S.C.T. MULTI PORT, INJECTION SITE?

The FDA product code for S.C.T. MULTI PORT, INJECTION SITE is FPA.

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Other records listing Salt Creek Medical Technologies 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.

K864683NEONATAL FEEDING KITK871042URINE METER, 250CCK871087S.C.M.T. PERFORATORK871075SCMT UMBILICAL CLAMPK864682SALT CREEK P.I. TRAYK864692EXTENSION SETS

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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.

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

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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