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FDA 510(k)

MPS GRAVITY FLOW CONTROL SET

K-Number: K983926 · 1999-01-20

ApplicantCritical Device Corp.
Decision Date1999-01-20
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MPS GRAVITY FLOW CONTROL SET is the device name listed in this FDA 510(k) record. The listed applicant is Critical Device Corp.. It received FDA 510(k) clearance on 1999-01-20 under 510(k) number K983926. 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 MPS GRAVITY FLOW CONTROL SET?

MPS GRAVITY FLOW CONTROL SET is a medical device that received FDA 510(k) clearance on 1999-01-20. The listed applicant is Critical Device Corp.. The 510(k) number is K983926.

When did MPS GRAVITY FLOW CONTROL SET receive FDA 510(k) clearance?

MPS GRAVITY FLOW CONTROL SET received FDA 510(k) clearance on 1999-01-20, under 510(k) number K983926.

Who is the listed applicant for MPS GRAVITY FLOW CONTROL SET?

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

What is the FDA product code for MPS GRAVITY FLOW CONTROL SET?

The FDA product code for MPS GRAVITY FLOW CONTROL SET 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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Other records listing Critical Device Corp. 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.

K964918NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER WITH POSIFLOW POSITIVE DISPLACEMENT FEATURE, AND I.V. SETSK964989CDC VIAL AND BAG ACCESS PIN (CDC-P-1/P-2/P-3/P-4/P-5)K964812NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SETK952852NIMA (NEEDLELESS INJECTIONSITE MASTER ADAPTER) & I.V. SETK955896MACROBORE TUBING - CDC-F-1 THROUGH CDC-F-11

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

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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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