STEALTH DILATION CATHETER SYSTEM/MODIFICATION
K-Number: K904287 · 1991-01-16
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Device Summary
Frequently Asked Questions
What is the STEALTH DILATION CATHETER SYSTEM/MODIFICATION?
STEALTH DILATION CATHETER SYSTEM/MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-01-16. The listed applicant is Target Therapeutics. The 510(k) number is K904287.
When did STEALTH DILATION CATHETER SYSTEM/MODIFICATION receive FDA 510(k) clearance?
STEALTH DILATION CATHETER SYSTEM/MODIFICATION received FDA 510(k) clearance on 1991-01-16, under 510(k) number K904287.
Who is the listed applicant for STEALTH DILATION CATHETER SYSTEM/MODIFICATION?
The FDA 510(k) record lists Target Therapeutics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STEALTH DILATION CATHETER SYSTEM/MODIFICATION?
The FDA product code for STEALTH DILATION CATHETER SYSTEM/MODIFICATION is DYG.
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 Target Therapeutics 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: DYG)
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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