MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER
K-Number: K960426 · 1996-03-21
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Device Summary
Frequently Asked Questions
What is the MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER?
MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Medical Components, Inc.. The 510(k) number is K960426.
When did MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER receive FDA 510(k) clearance?
MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER received FDA 510(k) clearance on 1996-03-21, under 510(k) number K960426.
Who is the listed applicant for MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER?
The FDA 510(k) record lists Medical Components, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER?
The FDA product code for MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER is GBW.
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 Medical Components, 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: GBW)
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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