Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ROSS-EMERSON PUMP, MODEL 55-R

K-Number: K811779 · 1981-07-13

ApplicantJ. H. Emerson Co.
Decision Date1981-07-13
Product CodeKQT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ROSS-EMERSON PUMP, MODEL 55-R 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 1981-07-13 under 510(k) number K811779. The device is classified under product code KQT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROSS-EMERSON PUMP, MODEL 55-R?

ROSS-EMERSON PUMP, MODEL 55-R is a medical device that received FDA 510(k) clearance on 1981-07-13. The listed applicant is J. H. Emerson Co.. The 510(k) number is K811779.

When did ROSS-EMERSON PUMP, MODEL 55-R receive FDA 510(k) clearance?

ROSS-EMERSON PUMP, MODEL 55-R received FDA 510(k) clearance on 1981-07-13, under 510(k) number K811779.

Who is the listed applicant for ROSS-EMERSON PUMP, MODEL 55-R?

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 ROSS-EMERSON PUMP, MODEL 55-R?

The FDA product code for ROSS-EMERSON PUMP, MODEL 55-R is KQT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 →

Related Devices (Code: KQT)

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.

K964111LITHOVAC SUCTION/ASPIRATION PROBEElectro Medical Systems SAK921088EVACUATOR, GASTRO-UROLOGYNorthgate Technologies, Inc.K921451EVACUATOR, GASTRO-UROLOGYNorthgate Technologies, Inc.K910728CLEANFLOW SYSTEMMitron Technologies, Inc.K880099VAN-TEC BLADDER EVACUATORVan-Tec, Inc.K874493BELLA - VAC IRRIGATORBel-Can Industries

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.

↑