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FDA 510(k)

NEEDLESAFE HANDGUARD

K-Number: K931813 · 1993-07-22

ApplicantAdrian Anesthesia Systems, Inc.
Decision Date1993-07-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLESAFE HANDGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Adrian Anesthesia Systems, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K931813. 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 NEEDLESAFE HANDGUARD?

NEEDLESAFE HANDGUARD is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Adrian Anesthesia Systems, Inc.. The 510(k) number is K931813.

When did NEEDLESAFE HANDGUARD receive FDA 510(k) clearance?

NEEDLESAFE HANDGUARD received FDA 510(k) clearance on 1993-07-22, under 510(k) number K931813.

Who is the listed applicant for NEEDLESAFE HANDGUARD?

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

What is the FDA product code for NEEDLESAFE HANDGUARD?

The FDA product code for NEEDLESAFE HANDGUARD 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

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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