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FDA 510(k)

L.O.N. REUSABLE MANIFOLDS & STOPCOCKS

K-Number: K812407 · 1981-12-02

ApplicantL.O.N. Research, Inc.
Decision Date1981-12-02
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

L.O.N. REUSABLE MANIFOLDS & STOPCOCKS is the device name listed in this FDA 510(k) record. The listed applicant is L.O.N. Research, Inc.. It received FDA 510(k) clearance on 1981-12-02 under 510(k) number K812407. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L.O.N. REUSABLE MANIFOLDS & STOPCOCKS?

L.O.N. REUSABLE MANIFOLDS & STOPCOCKS is a medical device that received FDA 510(k) clearance on 1981-12-02. The listed applicant is L.O.N. Research, Inc.. The 510(k) number is K812407.

When did L.O.N. REUSABLE MANIFOLDS & STOPCOCKS receive FDA 510(k) clearance?

L.O.N. REUSABLE MANIFOLDS & STOPCOCKS received FDA 510(k) clearance on 1981-12-02, under 510(k) number K812407.

Who is the listed applicant for L.O.N. REUSABLE MANIFOLDS & STOPCOCKS?

The FDA 510(k) record lists L.O.N. Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L.O.N. REUSABLE MANIFOLDS & STOPCOCKS?

The FDA product code for L.O.N. REUSABLE MANIFOLDS & STOPCOCKS is DTL.

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.

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Other records listing L.O.N. Research, Inc. 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.

K890676DISPOSABLE TRANSDUCER MANIFOLDK880158ANGIOPLASTY BALLOON INFLATION DEVICEK853099L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATIONK812408L.O.N. DISPOSABLE CORONARY MANIFOLD

Related Devices (Code: DTL)

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.

K131124COLIGNJilin Coronado Medical , Ltd.K123448AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH BALANCE BIOSURFACE, AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH CARMEDA BIOACTIVEMedtronic, Inc.K122811CONNECTOR COMPONENTS WITH BALANCE BIOSURFACEMedtronic, Inc.K122301GUARDIAN II HEMOSTASIS VALVE GUARDIAN II NC HEMOSTASIS VALVEVascular Solutions Zerusa , Ltd.K120069MEDLINE STOPCOCK AND MANIFOLDMedline Industries, Inc.K113148E-PASSSynexmed(Shenzhen)Company Limited

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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