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FDA 510(k)

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA

K-Number: K932411 · 1994-09-19

Decision Date1994-09-19
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA 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 1994-09-19 under 510(k) number K932411. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA?

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA is a medical device that received FDA 510(k) clearance on 1994-09-19. The listed applicant is Med Institute, Inc.. The 510(k) number is K932411.

When did VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA receive FDA 510(k) clearance?

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA received FDA 510(k) clearance on 1994-09-19, under 510(k) number K932411.

Who is the listed applicant for VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA?

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 VASC ACCESS SYS W/DUAL LUM INJECTROL CA?

The FDA product code for VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA is LJT.

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 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: LJT)

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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