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FDA 510(k)

EMERSON MODEL 3MV-OAA ALARM MODULE

K-Number: K854799 · 1985-12-11

ApplicantJ. H. Emerson Co.
Decision Date1985-12-11
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERSON MODEL 3MV-OAA ALARM MODULE 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 1985-12-11 under 510(k) number K854799. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERSON MODEL 3MV-OAA ALARM MODULE?

EMERSON MODEL 3MV-OAA ALARM MODULE is a medical device that received FDA 510(k) clearance on 1985-12-11. The listed applicant is J. H. Emerson Co.. The 510(k) number is K854799.

When did EMERSON MODEL 3MV-OAA ALARM MODULE receive FDA 510(k) clearance?

EMERSON MODEL 3MV-OAA ALARM MODULE received FDA 510(k) clearance on 1985-12-11, under 510(k) number K854799.

Who is the listed applicant for EMERSON MODEL 3MV-OAA ALARM MODULE?

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 3MV-OAA ALARM MODULE?

The FDA product code for EMERSON MODEL 3MV-OAA ALARM MODULE is CCL.

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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

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Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, Inc.

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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