ILT 0.014 CATHETER, MODEL C114NL2
K-Number: K001992 · 2000-09-25
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Device Summary
Frequently Asked Questions
What is the ILT 0.014 CATHETER, MODEL C114NL2?
ILT 0.014 CATHETER, MODEL C114NL2 is a medical device that received FDA 510(k) clearance on 2000-09-25. The listed applicant is Intra Luminal Therapeutics, Inc.. The 510(k) number is K001992.
When did ILT 0.014 CATHETER, MODEL C114NL2 receive FDA 510(k) clearance?
ILT 0.014 CATHETER, MODEL C114NL2 received FDA 510(k) clearance on 2000-09-25, under 510(k) number K001992.
Who is the listed applicant for ILT 0.014 CATHETER, MODEL C114NL2?
The FDA 510(k) record lists Intra Luminal Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ILT 0.014 CATHETER, MODEL C114NL2?
The FDA product code for ILT 0.014 CATHETER, MODEL C114NL2 is DQY.
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 Intra Luminal Therapeutics, 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: DQY)
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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