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FDA 510(k)

OXEQUIP CONDUCTIVE & NON ANES. BREATH

K-Number: K812624 · 1981-10-26

ApplicantOxequip Health Ind.
Decision Date1981-10-26
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXEQUIP CONDUCTIVE & NON ANES. BREATH 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 1981-10-26 under 510(k) number K812624. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXEQUIP CONDUCTIVE & NON ANES. BREATH?

OXEQUIP CONDUCTIVE & NON ANES. BREATH is a medical device that received FDA 510(k) clearance on 1981-10-26. The listed applicant is Oxequip Health Ind.. The 510(k) number is K812624.

When did OXEQUIP CONDUCTIVE & NON ANES. BREATH receive FDA 510(k) clearance?

OXEQUIP CONDUCTIVE & NON ANES. BREATH received FDA 510(k) clearance on 1981-10-26, under 510(k) number K812624.

Who is the listed applicant for OXEQUIP CONDUCTIVE & NON ANES. BREATH?

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 OXEQUIP CONDUCTIVE & NON ANES. BREATH?

The FDA product code for OXEQUIP CONDUCTIVE & NON ANES. BREATH is CAI.

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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/CONTROLLERK811987OXY-QUIK MARK IV OXYGEN INHALATORK800369TRI PAC MOUTH PROPK792356OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR

Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

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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