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FDA 510(k)

VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT

K-Number: K861563 · 1986-08-27

Decision Date1986-08-27
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1986-08-27 under 510(k) number K861563. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 13 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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