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)

EO EVACUATING SYSTEM I

K-Number: K790677 · 1979-05-07

ApplicantCastle Co.
Decision Date1979-05-07
Product CodeFLI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EO EVACUATING SYSTEM I is the device name listed in this FDA 510(k) record. The listed applicant is Castle Co.. It received FDA 510(k) clearance on 1979-05-07 under 510(k) number K790677. The device is classified under product code FLI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EO EVACUATING SYSTEM I?

EO EVACUATING SYSTEM I is a medical device that received FDA 510(k) clearance on 1979-05-07. The listed applicant is Castle Co.. The 510(k) number is K790677.

When did EO EVACUATING SYSTEM I receive FDA 510(k) clearance?

EO EVACUATING SYSTEM I received FDA 510(k) clearance on 1979-05-07, under 510(k) number K790677.

Who is the listed applicant for EO EVACUATING SYSTEM I?

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

What is the FDA product code for EO EVACUATING SYSTEM I?

The FDA product code for EO EVACUATING SYSTEM I is FLI.

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 Castle 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.

K870975MODIFIED CASTLE POWERCLAVEK860263CASTLE 7538 FLOOR LOADING WASHERK844089CASTLE 7515 UTENSIL/GLASSWARE WASHERK834048BOVIE CONDUCTIVE ADHES-DISPER-ELECTROK833074CASTLE TEC-TEST S.M.A.R.T. PACKK831595CASTLE MODEL 3341 & 3441 & 4141 GAS AER

View all 21 devices →

Related Devices (Code: FLI)

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.

K904921STERI-VAC(TM) AERATOR MODEL XL3M Health Care, Ltd.K902906GAS-VAK(R) COMBINATION STERILIZER & VENTILATORGas-VakK831595CASTLE MODEL 3341 & 3441 & 4141 GAS AERCastle Co.K830165BEAR JET 150 VENTILATORBear Medical Systems, Inc.K813201CASTLE #3241 GAS AERATORSybron Corp.K781484CASTLE MODEL 3146 GAS AERATORCastle Co.

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.

↑