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FDA 510(k)

OXY-QUIK MARK IV OXYGEN INHALATOR

K-Number: K811987 · 1981-07-27

ApplicantOxequip Health Ind.
Decision Date1981-07-27
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXY-QUIK MARK IV OXYGEN INHALATOR is the device name listed in this FDA 510(k) record. The listed applicant is Oxequip Health Ind.. It received FDA 510(k) clearance on 1981-07-27 under 510(k) number K811987. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXY-QUIK MARK IV OXYGEN INHALATOR?

OXY-QUIK MARK IV OXYGEN INHALATOR is a medical device that received FDA 510(k) clearance on 1981-07-27. The listed applicant is Oxequip Health Ind.. The 510(k) number is K811987.

When did OXY-QUIK MARK IV OXYGEN INHALATOR receive FDA 510(k) clearance?

OXY-QUIK MARK IV OXYGEN INHALATOR received FDA 510(k) clearance on 1981-07-27, under 510(k) number K811987.

Who is the listed applicant for OXY-QUIK MARK IV OXYGEN INHALATOR?

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

What is the FDA product code for OXY-QUIK MARK IV OXYGEN INHALATOR?

The FDA product code for OXY-QUIK MARK IV OXYGEN INHALATOR is DRM.

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.

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Other records listing Oxequip Health Ind. 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.

K833496OXYGEN MONITOR/CONTROLLERK812624OXEQUIP CONDUCTIVE & NON ANES. BREATHK800369TRI PAC MOUTH PROPK792356OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR

Related Devices (Code: DRM)

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.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

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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