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FDA 510(k)

EMERSON THORACIC SUCTION REG. #55-JP

K-Number: K820077 · 1982-01-28

ApplicantJ. H. Emerson Co.
Decision Date1982-01-28
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMERSON THORACIC SUCTION REG. #55-JP 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 1982-01-28 under 510(k) number K820077. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERSON THORACIC SUCTION REG. #55-JP?

EMERSON THORACIC SUCTION REG. #55-JP is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is J. H. Emerson Co.. The 510(k) number is K820077.

When did EMERSON THORACIC SUCTION REG. #55-JP receive FDA 510(k) clearance?

EMERSON THORACIC SUCTION REG. #55-JP received FDA 510(k) clearance on 1982-01-28, under 510(k) number K820077.

Who is the listed applicant for EMERSON THORACIC SUCTION REG. #55-JP?

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 THORACIC SUCTION REG. #55-JP?

The FDA product code for EMERSON THORACIC SUCTION REG. #55-JP is KDP.

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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: KDP)

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.

K013976BOEHRINGER MRI SUCTION REGULATORYBoehringer LaboratoriesK944479PM3300 INTERMITTENT VACUUMPrecision Medical, Inc.K942747MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) )Engineered Orthopedic Technologies, Inc.K933232BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIEDBoehringer LaboratoriesK926140VACUUM POWER BODY FLUID SUCTION APPARATUSHill-Rom, Inc.K922817PM3000 & PM3100 VACUUM REGULATORPrecision Medical, 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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