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FDA 510(k)

EMERSON MODEL 3HV COMPACT VENTILATOR

K-Number: K862712 · 1986-09-18

Decision Date1986-09-18
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERSON MODEL 3HV COMPACT VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1986-09-18 under 510(k) number K862712. 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 EMERSON MODEL 3HV COMPACT VENTILATOR?

EMERSON MODEL 3HV COMPACT VENTILATOR is a medical device that received FDA 510(k) clearance on 1986-09-18. The listed applicant is J. H. Emerson Co.. The 510(k) number is K862712.

When did EMERSON MODEL 3HV COMPACT VENTILATOR receive FDA 510(k) clearance?

EMERSON MODEL 3HV COMPACT VENTILATOR received FDA 510(k) clearance on 1986-09-18, under 510(k) number K862712.

Who is the listed applicant for EMERSON MODEL 3HV COMPACT VENTILATOR?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERSON MODEL 3HV COMPACT VENTILATOR?

The FDA product code for EMERSON MODEL 3HV COMPACT 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.

Other records listing J. H. Emerson Co. 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.

View all 25 devices →

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

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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