ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER
K-Number: K950201 · 1995-12-15
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Device Summary
Frequently Asked Questions
What is the ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER?
ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER is a medical device that received FDA 510(k) clearance on 1995-12-15. The listed applicant is Sherwood Medical Co.. The 510(k) number is K950201.
When did ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER receive FDA 510(k) clearance?
ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER received FDA 510(k) clearance on 1995-12-15, under 510(k) number K950201.
Who is the listed applicant for ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER?
The FDA product code for ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER is JOL.
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 Sherwood Medical Co. 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: JOL)
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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