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FDA 510(k)

MPC-150 MALE TO MALE LUER ADAPTER

K-Number: K925930 · 1993-08-16

ApplicantMolded Products, Inc.
Decision Date1993-08-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MPC-150 MALE TO MALE LUER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Molded Products, Inc.. It received FDA 510(k) clearance on 1993-08-16 under 510(k) number K925930. 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 MPC-150 MALE TO MALE LUER ADAPTER?

MPC-150 MALE TO MALE LUER ADAPTER is a medical device that received FDA 510(k) clearance on 1993-08-16. The listed applicant is Molded Products, Inc.. The 510(k) number is K925930.

When did MPC-150 MALE TO MALE LUER ADAPTER receive FDA 510(k) clearance?

MPC-150 MALE TO MALE LUER ADAPTER received FDA 510(k) clearance on 1993-08-16, under 510(k) number K925930.

Who is the listed applicant for MPC-150 MALE TO MALE LUER ADAPTER?

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

What is the FDA product code for MPC-150 MALE TO MALE LUER ADAPTER?

The FDA product code for MPC-150 MALE TO MALE LUER ADAPTER is FPA.

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Other records listing Molded Products, 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.

K022068TUBING, DIALYSATE (AND CONNECTOR)K010366DISPOSABLE STORAGE CAPK010712DIALYSATE LINE WITH CONNECTORS/RE-USE WASH-OUT LINESK003712MODIFICATION TO MALE TO MALE LUER ADAPTERK925978MPC-80 TRANSDUCERK925927MPC-1000 INJECTION CAP/PLUG

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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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