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)

DISPOSABLE, PRESSURE RELIEF VALVE

K-Number: K840276 · 1984-04-23

ApplicantHospitak, Inc.
Decision Date1984-04-23
Product Code
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE, PRESSURE RELIEF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K840276. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE, PRESSURE RELIEF VALVE?

DISPOSABLE, PRESSURE RELIEF VALVE is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Hospitak, Inc.. The 510(k) number is K840276.

When did DISPOSABLE, PRESSURE RELIEF VALVE receive FDA 510(k) clearance?

DISPOSABLE, PRESSURE RELIEF VALVE received FDA 510(k) clearance on 1984-04-23, under 510(k) number K840276.

Who is the listed applicant for DISPOSABLE, PRESSURE RELIEF VALVE?

The FDA 510(k) record lists Hospitak, Inc. 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_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 Hospitak, Inc. 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.

K955483TRACH MASK MODEL (245, 246)K954787ILLUMINATORK953619WARM N WET HME W/LUER ADAPTERK953620WARM N WET HMEF W/LUER ADAPTERK915750DISPOSABLE BACTERIAL BREATHNG FILTERK920842AEROSOL DELIVERY SYSTEMS

View all 27 devices →

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.

↑