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FDA 510(k)

PRO-LOK EXTENSION SET

K-Number: K933852 · 1993-12-29

ApplicantBeech Medical Products, Inc.
Decision Date1993-12-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO-LOK EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Beech Medical Products, Inc.. It received FDA 510(k) clearance on 1993-12-29 under 510(k) number K933852. 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 PRO-LOK EXTENSION SET?

PRO-LOK EXTENSION SET is a medical device that received FDA 510(k) clearance on 1993-12-29. The listed applicant is Beech Medical Products, Inc.. The 510(k) number is K933852.

When did PRO-LOK EXTENSION SET receive FDA 510(k) clearance?

PRO-LOK EXTENSION SET received FDA 510(k) clearance on 1993-12-29, under 510(k) number K933852.

Who is the listed applicant for PRO-LOK EXTENSION SET?

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

What is the FDA product code for PRO-LOK EXTENSION SET?

The FDA product code for PRO-LOK EXTENSION SET is FPA.

Related Clinical Trials

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.

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Other records listing Beech Medical 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.

K972469SELFSHIELD HN SELF SHEATHING HYPODERMIC NEEDLEK946082BEECH PRO LOK FIXEDK933749BEECH VERSA LOK

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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