CYPERFLO PERIPHERALLY INSERTED CATHETER
K-Number: K935145 · 1995-03-09
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Device Summary
Frequently Asked Questions
What is the CYPERFLO PERIPHERALLY INSERTED CATHETER?
CYPERFLO PERIPHERALLY INSERTED CATHETER is a medical device that received FDA 510(k) clearance on 1995-03-09. The listed applicant is Cyex Medical Technologies, Inc.. The 510(k) number is K935145.
When did CYPERFLO PERIPHERALLY INSERTED CATHETER receive FDA 510(k) clearance?
CYPERFLO PERIPHERALLY INSERTED CATHETER received FDA 510(k) clearance on 1995-03-09, under 510(k) number K935145.
Who is the listed applicant for CYPERFLO PERIPHERALLY INSERTED CATHETER?
The FDA 510(k) record lists Cyex Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CYPERFLO PERIPHERALLY INSERTED CATHETER?
The FDA product code for CYPERFLO 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 Cyex Medical Technologies, 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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