FDA 510(k)

ERIE OXYGEN CONCENTRATOR

K-Number: K822719 · 1982-09-28

Decision Date1982-09-28

Product Code

DecisionSubstantially Equivalent

Device Summary

ERIE OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Erie Controls. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822719. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERIE OXYGEN CONCENTRATOR?

ERIE OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Erie Controls. The 510(k) number is K822719.

When did ERIE OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

ERIE OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822719.

Who is the listed applicant for ERIE OXYGEN CONCENTRATOR?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.