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FDA 510(k)

EXTENTION SET

K-Number: K933524 · 1995-05-23

ApplicantMediziv Medical Products 1987 , Ltd.
Decision Date1995-05-23
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTENTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Mediziv Medical Products 1987 , Ltd.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K933524. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENTION SET?

EXTENTION SET is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Mediziv Medical Products 1987 , Ltd.. The 510(k) number is K933524.

When did EXTENTION SET receive FDA 510(k) clearance?

EXTENTION SET received FDA 510(k) clearance on 1995-05-23, under 510(k) number K933524.

Who is the listed applicant for EXTENTION SET?

The FDA 510(k) record lists Mediziv Medical Products 1987 , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTENTION SET?

The FDA product code for EXTENTION SET is FPK.

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 Mediziv Medical Products 1987 , Ltd. 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.

K933898HUBER NEEDLE SETSK933523I.V. FILTER SETK933522INTRODUCER NEEDLE (SEVERAL SIZES)

Related Devices (Code: FPK)

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.

K131517MEDRAD TWIST & GO HIGH PRESSURE CONNECTOR TUBINGMedrad, Inc. / Bayer Medical Care, Inc.K063114DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVESCoeur, Inc.K063239LIFESHIELD LATEX-FREE GRAVITECH FLOW CONTROLLER I.V. SETS, MODELS 17528, 17527, 17525 & 17526Hospira, Inc.K052431MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1Medtronic MinimedK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)E-Z-Em, Inc.K031808MEDRAD SWABBABLE VALVE TRANSFER SETMedrad, Inc.

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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