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FDA 510(k)

WALL IV EXTENSION TUBE

K-Number: K940689 · 1994-03-22

ApplicantWalla Medical Systems, Inc.
Decision Date1994-03-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WALL IV EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Walla Medical Systems, Inc.. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K940689. 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 WALL IV EXTENSION TUBE?

WALL IV EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Walla Medical Systems, Inc.. The 510(k) number is K940689.

When did WALL IV EXTENSION TUBE receive FDA 510(k) clearance?

WALL IV EXTENSION TUBE received FDA 510(k) clearance on 1994-03-22, under 510(k) number K940689.

Who is the listed applicant for WALL IV EXTENSION TUBE?

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

What is the FDA product code for WALL IV EXTENSION TUBE?

The FDA product code for WALL IV EXTENSION TUBE is FPA.

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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

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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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