VIP PLUS PERCUTANEOUS INTRODUCER
K-Number: K944107 · 1994-09-14
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Device Summary
Frequently Asked Questions
What is the VIP PLUS PERCUTANEOUS INTRODUCER?
VIP PLUS PERCUTANEOUS INTRODUCER is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Medamicus, Inc.. The 510(k) number is K944107.
When did VIP PLUS PERCUTANEOUS INTRODUCER receive FDA 510(k) clearance?
VIP PLUS PERCUTANEOUS INTRODUCER received FDA 510(k) clearance on 1994-09-14, under 510(k) number K944107.
Who is the listed applicant for VIP PLUS PERCUTANEOUS INTRODUCER?
The FDA 510(k) record lists Medamicus, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIP PLUS PERCUTANEOUS INTRODUCER?
The FDA product code for VIP PLUS PERCUTANEOUS INTRODUCER is DYB.
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 Medamicus, 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: DYB)
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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