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FDA 510(k)

VECTOR

K-Number: K002122 · 2000-12-21

ApplicantAir Techniques, Inc.
Decision Date2000-12-21
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Air Techniques, Inc.. It received FDA 510(k) clearance on 2000-12-21 under 510(k) number K002122. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTOR?

VECTOR is a medical device that received FDA 510(k) clearance on 2000-12-21. The listed applicant is Air Techniques, Inc.. The 510(k) number is K002122.

When did VECTOR receive FDA 510(k) clearance?

VECTOR received FDA 510(k) clearance on 2000-12-21, under 510(k) number K002122.

Who is the listed applicant for VECTOR?

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

What is the FDA product code for VECTOR?

The FDA product code for VECTOR is ELC.

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Related PubMed Literature

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PMID: 30005090Straight-Line Vector Planning for Optimal Results With Silhouette InstaLift in Minimally Invasive Tissue Repositioning for Facial Rejuvenation.Journal of drugs in dermatology : JDD ()

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Related Devices (Code: ELC)

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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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