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FDA 510(k)

SILASTIC INTRAVENOUS CATHETER UNIT

K-Number: K790914 · 1979-07-03

ApplicantDow Corning Corp. Healthcare Industries Materials
Decision Date1979-07-03
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SILASTIC INTRAVENOUS CATHETER UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K790914. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC INTRAVENOUS CATHETER UNIT?

SILASTIC INTRAVENOUS CATHETER UNIT is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K790914.

When did SILASTIC INTRAVENOUS CATHETER UNIT receive FDA 510(k) clearance?

SILASTIC INTRAVENOUS CATHETER UNIT received FDA 510(k) clearance on 1979-07-03, under 510(k) number K790914.

Who is the listed applicant for SILASTIC INTRAVENOUS CATHETER UNIT?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILASTIC INTRAVENOUS CATHETER UNIT?

The FDA product code for SILASTIC INTRAVENOUS CATHETER UNIT is FOZ.

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Other records listing Dow Corning Corp. Healthcare Industries Materials as applicant

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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