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FDA 510(k)

MPC-1000 INJECTION CAP/PLUG

K-Number: K925927 · 1993-08-16

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

Device Summary

MPC-1000 INJECTION CAP/PLUG 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 K925927. 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-1000 INJECTION CAP/PLUG?

MPC-1000 INJECTION CAP/PLUG 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 K925927.

When did MPC-1000 INJECTION CAP/PLUG receive FDA 510(k) clearance?

MPC-1000 INJECTION CAP/PLUG received FDA 510(k) clearance on 1993-08-16, under 510(k) number K925927.

Who is the listed applicant for MPC-1000 INJECTION CAP/PLUG?

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-1000 INJECTION CAP/PLUG?

The FDA product code for MPC-1000 INJECTION CAP/PLUG 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 TRANSDUCERK925930MPC-150 MALE TO MALE LUER ADAPTER

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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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