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FDA 510(k)

SIDEPORT PINCH CLAMP DEVICE

K-Number: K010888 · 2001-06-27

ApplicantMedivice Systems, Ltd.
Decision Date2001-06-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIDEPORT PINCH CLAMP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medivice Systems, Ltd.. It received FDA 510(k) clearance on 2001-06-27 under 510(k) number K010888. 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 SIDEPORT PINCH CLAMP DEVICE?

SIDEPORT PINCH CLAMP DEVICE is a medical device that received FDA 510(k) clearance on 2001-06-27. The listed applicant is Medivice Systems, Ltd.. The 510(k) number is K010888.

When did SIDEPORT PINCH CLAMP DEVICE receive FDA 510(k) clearance?

SIDEPORT PINCH CLAMP DEVICE received FDA 510(k) clearance on 2001-06-27, under 510(k) number K010888.

Who is the listed applicant for SIDEPORT PINCH CLAMP DEVICE?

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

What is the FDA product code for SIDEPORT PINCH CLAMP DEVICE?

The FDA product code for SIDEPORT PINCH CLAMP DEVICE is FPA.

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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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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