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FDA 510(k)

PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT

K-Number: K904334 · 1990-11-05

Decision Date1990-11-05
Product CodeLJS
Advisory CommitteeHO
DecisionUnknown

Device Summary

PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K904334. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT?

PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K904334.

When did PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT receive FDA 510(k) clearance?

PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT received FDA 510(k) clearance on 1990-11-05, under 510(k) number K904334.

Who is the listed applicant for PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT?

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

What is the FDA product code for PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT?

The FDA product code for PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT is LJS.

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.

Other records listing Pharmacia Deltec, 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.

View all 43 devices →

Related Devices (Code: LJS)

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.

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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