CLINICATH IR PERIPHERALLY INSERTED CATHETER
K-Number: K970269 · 1997-06-26
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Device Summary
Frequently Asked Questions
What is the CLINICATH IR PERIPHERALLY INSERTED CATHETER?
CLINICATH IR PERIPHERALLY INSERTED CATHETER is a medical device that received FDA 510(k) clearance on 1997-06-26. The listed applicant is Sims Deltec, Inc.. The 510(k) number is K970269.
When did CLINICATH IR PERIPHERALLY INSERTED CATHETER receive FDA 510(k) clearance?
CLINICATH IR PERIPHERALLY INSERTED CATHETER received FDA 510(k) clearance on 1997-06-26, under 510(k) number K970269.
Who is the listed applicant for CLINICATH IR PERIPHERALLY INSERTED CATHETER?
The FDA 510(k) record lists Sims Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINICATH IR PERIPHERALLY INSERTED CATHETER?
The FDA product code for CLINICATH IR PERIPHERALLY INSERTED CATHETER 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 Sims 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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