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FDA 510(k)

I.V. CATHETER PLACEMENT UNIT

K-Number: K770181 · 1977-03-30

ApplicantAmerican Viggo
Decision Date1977-03-30
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

I.V. CATHETER PLACEMENT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is American Viggo. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770181. 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 I.V. CATHETER PLACEMENT UNIT?

I.V. CATHETER PLACEMENT UNIT is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is American Viggo. The 510(k) number is K770181.

When did I.V. CATHETER PLACEMENT UNIT receive FDA 510(k) clearance?

I.V. CATHETER PLACEMENT UNIT received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770181.

Who is the listed applicant for I.V. CATHETER PLACEMENT UNIT?

The FDA 510(k) record lists American Viggo as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. CATHETER PLACEMENT UNIT?

The FDA product code for I.V. CATHETER PLACEMENT UNIT is FOZ.

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Other records listing American Viggo 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.

K771339MALE LUER LOCK PLUGK770528NEEDLE, MEMBRANEK770174LUER-LOCK EXTENSION SETK7701543-WAY STOPCOCK WITH LUER-LOCK FITTINGK770096EPIDURAL BLOCK PROCEDURE PACKK7606794-WAY STOPCOCK W/7CM TUBING,

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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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