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FDA 510(k)

LOW PRESSURE ALARM FOR OXYGEN CYLINDER

K-Number: K843212 · 1984-09-19

ApplicantHospitak, Inc.
Decision Date1984-09-19
Product CodeBXH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LOW PRESSURE ALARM FOR OXYGEN CYLINDER is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1984-09-19 under 510(k) number K843212. The device is classified under product code BXH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW PRESSURE ALARM FOR OXYGEN CYLINDER?

LOW PRESSURE ALARM FOR OXYGEN CYLINDER is a medical device that received FDA 510(k) clearance on 1984-09-19. The listed applicant is Hospitak, Inc.. The 510(k) number is K843212.

When did LOW PRESSURE ALARM FOR OXYGEN CYLINDER receive FDA 510(k) clearance?

LOW PRESSURE ALARM FOR OXYGEN CYLINDER received FDA 510(k) clearance on 1984-09-19, under 510(k) number K843212.

Who is the listed applicant for LOW PRESSURE ALARM FOR OXYGEN CYLINDER?

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

What is the FDA product code for LOW PRESSURE ALARM FOR OXYGEN CYLINDER?

The FDA product code for LOW PRESSURE ALARM FOR OXYGEN CYLINDER is BXH.

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Other records listing Hospitak, Inc. as applicant

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

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Related Devices (Code: BXH)

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.

K942645B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REGB & F Medical Products, Inc.K853040PRESSURE GAUGEErie MedicalK770614MONITOR, GAS MANIFOLDDynatech Cryomedical 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.

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