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FDA 510(k)

VECTOR SEIGE 2023645 AC POWERED STIMU-

K-Number: K833305 · 1983-11-28

Decision Date1983-11-28
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VECTOR SEIGE 2023645 AC POWERED STIMU- is the device name listed in this FDA 510(k) record. The listed applicant is Metronex Engineering. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833305. 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 VECTOR SEIGE 2023645 AC POWERED STIMU-?

VECTOR SEIGE 2023645 AC POWERED STIMU- is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Metronex Engineering. The 510(k) number is K833305.

When did VECTOR SEIGE 2023645 AC POWERED STIMU- receive FDA 510(k) clearance?

VECTOR SEIGE 2023645 AC POWERED STIMU- received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833305.

Who is the listed applicant for VECTOR SEIGE 2023645 AC POWERED STIMU-?

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

What is the FDA product code for VECTOR SEIGE 2023645 AC POWERED STIMU-?

The FDA product code for VECTOR SEIGE 2023645 AC POWERED STIMU- 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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