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FDA 510(k)

INFUSION SET, VENOTHIN 21

K-Number: K781190 · 1978-08-10

ApplicantVenospital, Inc.
Decision Date1978-08-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION SET, VENOTHIN 21 is the device name listed in this FDA 510(k) record. The listed applicant is Venospital, Inc.. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K781190. 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 INFUSION SET, VENOTHIN 21?

INFUSION SET, VENOTHIN 21 is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Venospital, Inc.. The 510(k) number is K781190.

When did INFUSION SET, VENOTHIN 21 receive FDA 510(k) clearance?

INFUSION SET, VENOTHIN 21 received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781190.

Who is the listed applicant for INFUSION SET, VENOTHIN 21?

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

What is the FDA product code for INFUSION SET, VENOTHIN 21?

The FDA product code for INFUSION SET, VENOTHIN 21 is FPA.

Related Clinical Trials

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Other records listing Venospital, 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.

K791131FLU VEN TR-1K791130FLU-VEN TK-2K790424FLU-VEN 01510K790077BIOSTIL # 3884K781186INFUSION, VENOTHIN 23K781185INFUSION SET W/ INJECTION SITE

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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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