PERCUTANEOUS INTRAVENOUS CATHETERS
K-Number: K895712 · 1989-12-15
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Device Summary
Frequently Asked Questions
What is the PERCUTANEOUS INTRAVENOUS CATHETERS?
PERCUTANEOUS INTRAVENOUS CATHETERS is a medical device that received FDA 510(k) clearance on 1989-12-15. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K895712.
When did PERCUTANEOUS INTRAVENOUS CATHETERS receive FDA 510(k) clearance?
PERCUTANEOUS INTRAVENOUS CATHETERS received FDA 510(k) clearance on 1989-12-15, under 510(k) number K895712.
Who is the listed applicant for PERCUTANEOUS INTRAVENOUS CATHETERS?
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 CATHETERS?
The FDA product code for PERCUTANEOUS INTRAVENOUS CATHETERS 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.
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
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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