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FDA 510(k)

PERCUTANEOUS INTRODUCER KIT

K-Number: K902135 · 1990-08-01

ApplicantDevice Labs, Inc.
Decision Date1990-08-01
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

PERCUTANEOUS INTRODUCER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Device Labs, Inc.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902135. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERCUTANEOUS INTRODUCER KIT?

PERCUTANEOUS INTRODUCER KIT is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Device Labs, Inc.. The 510(k) number is K902135.

When did PERCUTANEOUS INTRODUCER KIT receive FDA 510(k) clearance?

PERCUTANEOUS INTRODUCER KIT received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902135.

Who is the listed applicant for PERCUTANEOUS INTRODUCER KIT?

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

What is the FDA product code for PERCUTANEOUS INTRODUCER KIT?

The FDA product code for PERCUTANEOUS INTRODUCER KIT is FOZ.

Related Clinical Trials

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Other records listing Device Labs, 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.

K930632CHEMOSITE IMPLANTABLE DRUG DELIVERYK904417CHEMOSITE IMPLANTABLE DRUG DELIVERY SYSTEMK901722CHEMOSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEMK883764INTRAVASCULAR ADMINISTRATION SETK882064LO-CORE NEEDLE

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

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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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