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FDA 510(k)

R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE

K-Number: K940319 · 1994-11-10

ApplicantR-Group Intl.
Decision Date1994-11-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE is the device name listed in this FDA 510(k) record. The listed applicant is R-Group Intl.. It received FDA 510(k) clearance on 1994-11-10 under 510(k) number K940319. 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 R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE?

R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE is a medical device that received FDA 510(k) clearance on 1994-11-10. The listed applicant is R-Group Intl.. The 510(k) number is K940319.

When did R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE receive FDA 510(k) clearance?

R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE received FDA 510(k) clearance on 1994-11-10, under 510(k) number K940319.

Who is the listed applicant for R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE?

The FDA 510(k) record lists R-Group Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE?

The FDA product code for R-GROUP INTERNATIONAL COILED LOW PRESSURE EXTENSION LINE is FPA.

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Other records listing R-Group Intl. 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.

K001233ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D SK001599ACTI-FLEX IV ADMINISTRATION SETK993777DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODESK952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.K954035ACTI-FLEX ARTERIAL EXTENSION SETK913267R-GROUP INTL. ONE WALL PUNCTURE NEEDLE

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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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