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FDA 510(k)

VIFI: VECTOR INTERFERENTIAL ONE

K-Number: K931732 · 1994-03-10

Decision Date1994-03-10
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIFI: VECTOR INTERFERENTIAL ONE is the device name listed in this FDA 510(k) record. The listed applicant is Compliance Technology, Inc.. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K931732. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIFI: VECTOR INTERFERENTIAL ONE?

VIFI: VECTOR INTERFERENTIAL ONE is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Compliance Technology, Inc.. The 510(k) number is K931732.

When did VIFI: VECTOR INTERFERENTIAL ONE receive FDA 510(k) clearance?

VIFI: VECTOR INTERFERENTIAL ONE received FDA 510(k) clearance on 1994-03-10, under 510(k) number K931732.

Who is the listed applicant for VIFI: VECTOR INTERFERENTIAL ONE?

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

What is the FDA product code for VIFI: VECTOR INTERFERENTIAL ONE?

The FDA product code for VIFI: VECTOR INTERFERENTIAL ONE is LIH.

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.

Related Devices (Code: LIH)

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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