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FDA 510(k)

EMERSON 3MV VOLUME VENTILATOR

K-Number: K864394 · 1986-12-05

ApplicantJ. H. Emerson Co.
Decision Date1986-12-05
Product Code
DecisionSubstantially Equivalent

Device Summary

EMERSON 3MV VOLUME 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 1986-12-05 under 510(k) number K864394. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERSON 3MV VOLUME VENTILATOR?

EMERSON 3MV VOLUME VENTILATOR is a medical device that received FDA 510(k) clearance on 1986-12-05. The listed applicant is J. H. Emerson Co.. The 510(k) number is K864394.

When did EMERSON 3MV VOLUME VENTILATOR receive FDA 510(k) clearance?

EMERSON 3MV VOLUME VENTILATOR received FDA 510(k) clearance on 1986-12-05, under 510(k) number K864394.

Who is the listed applicant for EMERSON 3MV VOLUME VENTILATOR?

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

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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.

K002598EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMINGK920910OXYGEN POWERED RESUSCITATOR FOR CPRK924174EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CAK902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMK896721MODEL 7-AT TREATMENT CHAMBERK881808EMERSON CHEST RESPIRATOR, MODEL 33-CRE

View all 25 devices →

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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