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FDA 510(k)

SOLOPICC 24 (60CM) 20GA CATHETER

K-Number: K954428 · 1996-03-28

ApplicantDouglas Medical Products Corp.
Decision Date1996-03-28
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLOPICC 24 (60CM) 20GA CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products Corp.. It received FDA 510(k) clearance on 1996-03-28 under 510(k) number K954428. 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 SOLOPICC 24 (60CM) 20GA CATHETER?

SOLOPICC 24 (60CM) 20GA CATHETER is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K954428.

When did SOLOPICC 24 (60CM) 20GA CATHETER receive FDA 510(k) clearance?

SOLOPICC 24 (60CM) 20GA CATHETER received FDA 510(k) clearance on 1996-03-28, under 510(k) number K954428.

Who is the listed applicant for SOLOPICC 24 (60CM) 20GA CATHETER?

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

What is the FDA product code for SOLOPICC 24 (60CM) 20GA CATHETER?

The FDA product code for SOLOPICC 24 (60CM) 20GA CATHETER is FOZ.

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Other records listing Douglas Medical Products Corp. 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.

K961155SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908K94162840 MICRON BLOOD TRANSFUSION FILTERK9421014-LEAD IRRIGATION SETK941453CHECK VALVE SOLUTION SETK930854SOLUTION SET WITH .2 MICRON FILTERK932637SUBCUTANEOUS INFUSION SET

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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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