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FDA 510(k)

VS600 JET VENTILATOR

K-Number: K812016 · 1981-12-30

Decision Date1981-12-30
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VS600 JET VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Instrument Development Corp.. It received FDA 510(k) clearance on 1981-12-30 under 510(k) number K812016. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VS600 JET VENTILATOR?

VS600 JET VENTILATOR is a medical device that received FDA 510(k) clearance on 1981-12-30. The listed applicant is Instrument Development Corp.. The 510(k) number is K812016.

When did VS600 JET VENTILATOR receive FDA 510(k) clearance?

VS600 JET VENTILATOR received FDA 510(k) clearance on 1981-12-30, under 510(k) number K812016.

Who is the listed applicant for VS600 JET VENTILATOR?

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

What is the FDA product code for VS600 JET VENTILATOR?

The FDA product code for VS600 JET VENTILATOR is CBK.

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: CBK)

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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