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FDA 510(k)

EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM

K-Number: K902764 · 1990-11-19

ApplicantJ. H. Emerson Co.
Decision Date1990-11-19
Product CodeBYT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM 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 1990-11-19 under 510(k) number K902764. The device is classified under product code BYT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM?

EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM is a medical device that received FDA 510(k) clearance on 1990-11-19. The listed applicant is J. H. Emerson Co.. The 510(k) number is K902764.

When did EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM receive FDA 510(k) clearance?

EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM received FDA 510(k) clearance on 1990-11-19, under 510(k) number K902764.

Who is the listed applicant for EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM?

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 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM?

The FDA product code for EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM is BYT.

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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-CAK896721MODEL 7-AT TREATMENT CHAMBERK881808EMERSON CHEST RESPIRATOR, MODEL 33-CREK873489EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000

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Related Devices (Code: BYT)

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.

K082657RTX RESPIRATORMedivent LimitedK072290PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUSDima Italia SrlK924341HAYEK OSCILLATOR(TM)Respironics, Inc.K910947NEV-10 NEGATIVE PRESSURE VENTILATORLifecare Services, Inc.K905530PURITAN-BENNETT COMPANION 500 LIQUID OXYGEN SYSTEMPuritan Bennett Corp.K903745THE HAYEK OSCILLATORFlexco Medical Instruments

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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