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FDA 510(k)

MINI-VOL I.V. SET

K-Number: K831088 · 1983-04-28

ApplicantBeech Medical, Inc.
Decision Date1983-04-28
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MINI-VOL I.V. SET is the device name listed in this FDA 510(k) record. The listed applicant is Beech Medical, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831088. 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 MINI-VOL I.V. SET?

MINI-VOL I.V. SET is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Beech Medical, Inc.. The 510(k) number is K831088.

When did MINI-VOL I.V. SET receive FDA 510(k) clearance?

MINI-VOL I.V. SET received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831088.

Who is the listed applicant for MINI-VOL I.V. SET?

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

What is the FDA product code for MINI-VOL I.V. SET?

The FDA product code for MINI-VOL I.V. SET is FPA.

Other records listing Beech Medical, 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.

K933732BEECH PROLOKK831089INFUSION PUMPK831087MINI-VOL EXTENSION SETK823373BENZING RETROGRADE ADMIN. SET

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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