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FDA 510(k)

MALE LUER LOCK PLUG

K-Number: K771339 · 1977-08-02

ApplicantAmerican Viggo
Decision Date1977-08-02
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MALE LUER LOCK PLUG is the device name listed in this FDA 510(k) record. The listed applicant is American Viggo. It received FDA 510(k) clearance on 1977-08-02 under 510(k) number K771339. 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 MALE LUER LOCK PLUG?

MALE LUER LOCK PLUG is a medical device that received FDA 510(k) clearance on 1977-08-02. The listed applicant is American Viggo. The 510(k) number is K771339.

When did MALE LUER LOCK PLUG receive FDA 510(k) clearance?

MALE LUER LOCK PLUG received FDA 510(k) clearance on 1977-08-02, under 510(k) number K771339.

Who is the listed applicant for MALE LUER LOCK PLUG?

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

What is the FDA product code for MALE LUER LOCK PLUG?

The FDA product code for MALE LUER LOCK PLUG is FPA.

Other records listing American Viggo 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.

K770528NEEDLE, MEMBRANEK770181I.V. CATHETER PLACEMENT UNITK770174LUER-LOCK EXTENSION SETK7701543-WAY STOPCOCK WITH LUER-LOCK FITTINGK770096EPIDURAL BLOCK PROCEDURE PACKK7606794-WAY STOPCOCK W/7CM TUBING,

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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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