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FDA 510(k)

VENTED SOLUTION SET

K-Number: K955732 · 1996-02-21

ApplicantDistronic Sterile Products, Inc.
Decision Date1996-02-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENTED SOLUTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Distronic Sterile Products, Inc.. It received FDA 510(k) clearance on 1996-02-21 under 510(k) number K955732. 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 VENTED SOLUTION SET?

VENTED SOLUTION SET is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is Distronic Sterile Products, Inc.. The 510(k) number is K955732.

When did VENTED SOLUTION SET receive FDA 510(k) clearance?

VENTED SOLUTION SET received FDA 510(k) clearance on 1996-02-21, under 510(k) number K955732.

Who is the listed applicant for VENTED SOLUTION SET?

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

What is the FDA product code for VENTED SOLUTION SET?

The FDA product code for VENTED SOLUTION SET is FPA.

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Other records listing Distronic Sterile 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.

K955709WINGED & SUBCUTANEOUS INFUSION SETSK954984MINIBORE STOPCOCK SETK954983EXTENSION SET WITH CHECK VALVEK952664SOLUTION ADMINISTRATION SETK950597CORE-RESISTANT HUBER INFUSION SET WITH Y-SITEK95266360 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON GILYRT, INJ. SITE, CLAMP

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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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