AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY)
K-Number: K862697 · 1986-12-05
Advertisement
Device Summary
Frequently Asked Questions
What is the AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY)?
AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY) is a medical device that received FDA 510(k) clearance on 1986-12-05. The listed applicant is Advanced Vascular Technologies, Inc.. The 510(k) number is K862697.
When did AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY) receive FDA 510(k) clearance?
AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY) received FDA 510(k) clearance on 1986-12-05, under 510(k) number K862697.
Who is the listed applicant for AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY)?
The FDA 510(k) record lists Advanced Vascular Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY)?
The FDA product code for AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY) is DSY.
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.
Related Devices (Code: DSY)
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.
Advertisement