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FDA 510(k)

VECTOR AMBULATORY DRUG DELIVERY SYSTEM

K-Number: K935461 · 1994-04-28

Decision Date1994-04-28
Product CodeFIH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VECTOR AMBULATORY DRUG DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Infusion Technology Intl.. It received FDA 510(k) clearance on 1994-04-28 under 510(k) number K935461. The device is classified under product code FIH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTOR AMBULATORY DRUG DELIVERY SYSTEM?

VECTOR AMBULATORY DRUG DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Infusion Technology Intl.. The 510(k) number is K935461.

When did VECTOR AMBULATORY DRUG DELIVERY SYSTEM receive FDA 510(k) clearance?

VECTOR AMBULATORY DRUG DELIVERY SYSTEM received FDA 510(k) clearance on 1994-04-28, under 510(k) number K935461.

Who is the listed applicant for VECTOR AMBULATORY DRUG DELIVERY SYSTEM?

The FDA 510(k) record lists Infusion Technology Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VECTOR AMBULATORY DRUG DELIVERY SYSTEM?

The FDA product code for VECTOR AMBULATORY DRUG DELIVERY SYSTEM is FIH.

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 Infusion Technology Intl. 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: FIH)

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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