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FDA 510(k)

VITAL-PORT MINI VASCULAR ACCESS SYSTEM

K-Number: K931586 · 1993-09-27

ApplicantMed Institute, Inc.
Decision Date1993-09-27
Product CodeDWF
Advisory CommitteeCV
DecisionUnknown

Device Summary

VITAL-PORT MINI VASCULAR ACCESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Med Institute, Inc.. It received FDA 510(k) clearance on 1993-09-27 under 510(k) number K931586. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VITAL-PORT MINI VASCULAR ACCESS SYSTEM?

VITAL-PORT MINI VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-27. The listed applicant is Med Institute, Inc.. The 510(k) number is K931586.

When did VITAL-PORT MINI VASCULAR ACCESS SYSTEM receive FDA 510(k) clearance?

VITAL-PORT MINI VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1993-09-27, under 510(k) number K931586.

Who is the listed applicant for VITAL-PORT MINI VASCULAR ACCESS SYSTEM?

The FDA 510(k) record lists Med Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAL-PORT MINI VASCULAR ACCESS SYSTEM?

The FDA product code for VITAL-PORT MINI VASCULAR ACCESS SYSTEM is DWF.

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Other records listing Med Institute, 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.

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Related Devices (Code: DWF)

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.

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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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