POLY PER-Q-CATH PICC CATHETERS
K-Number: K034019 · 2004-01-21
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Device Summary
Frequently Asked Questions
What is the POLY PER-Q-CATH PICC CATHETERS?
POLY PER-Q-CATH PICC CATHETERS is a medical device that received FDA 510(k) clearance on 2004-01-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K034019.
When did POLY PER-Q-CATH PICC CATHETERS receive FDA 510(k) clearance?
POLY PER-Q-CATH PICC CATHETERS received FDA 510(k) clearance on 2004-01-21, under 510(k) number K034019.
Who is the listed applicant for POLY PER-Q-CATH PICC CATHETERS?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLY PER-Q-CATH PICC CATHETERS?
The FDA product code for POLY PER-Q-CATH PICC 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 C.R. Bard, 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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