OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1
K-Number: K920908 · 1992-10-06
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Device Summary
Frequently Asked Questions
What is the OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1?
OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1 is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K920908.
When did OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1 receive FDA 510(k) clearance?
OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1 received FDA 510(k) clearance on 1992-10-06, under 510(k) number K920908.
Who is the listed applicant for OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1?
The FDA 510(k) record lists Teleflexmedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1?
The FDA product code for OVER THE NEEDLE SPLITABLE CATHETER ASSEMBLY TYPE 1 is DYB.
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 Teleflexmedical, 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: DYB)
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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