VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT
K-Number: K861563 · 1986-08-27
Advertisement
Device Summary
Frequently Asked Questions
What is the VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT?
VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT is a medical device that received FDA 510(k) clearance on 1986-08-27. The listed applicant is Vitaphore Corp.. The 510(k) number is K861563.
When did VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT receive FDA 510(k) clearance?
VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT received FDA 510(k) clearance on 1986-08-27, under 510(k) number K861563.
Who is the listed applicant for VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT?
The FDA 510(k) record lists Vitaphore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT?
The FDA product code for VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT is LJS.
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 Vitaphore Corp. 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: LJS)
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