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FDA 510(k)

V SET

K-Number: K900336 · 1990-10-04

ApplicantGo Medical Industries Pty. , Ltd.
Decision Date1990-10-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V SET is the device name listed in this FDA 510(k) record. The listed applicant is Go Medical Industries Pty. , Ltd.. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K900336. 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 V SET?

V SET is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Go Medical Industries Pty. , Ltd.. The 510(k) number is K900336.

When did V SET receive FDA 510(k) clearance?

V SET received FDA 510(k) clearance on 1990-10-04, under 510(k) number K900336.

Who is the listed applicant for V SET?

The FDA 510(k) record lists Go Medical Industries Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V SET?

The FDA product code for V SET is FPA.

Other records listing Go Medical Industries Pty. , Ltd. 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.

K011055THE O'NEIL STERILE FIELD URINARY CATHETER KIT WITH PREP PADSK002803THE O'NEIL STERILE FIELD URINARY CATHETER KITK000263GO MEDICAL BALLOON INFUSION SYSTEMK910007SPRINGFUSOR 10RK895594SINGLE LUMEN O'NEIL ASPIRATION & IRRIGATION NEEDLEK890400MODIFIED URINARY CATHETER INTRODUCER (UCI)

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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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