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FDA 510(k)

COAXIAL VOL. VENTILATOR CIRCUIT

K-Number: K833459 · 1984-01-10

ApplicantAirco/Ohio Medical Products
Decision Date1984-01-10
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COAXIAL VOL. VENTILATOR CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Airco/Ohio Medical Products. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K833459. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAXIAL VOL. VENTILATOR CIRCUIT?

COAXIAL VOL. VENTILATOR CIRCUIT is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Airco/Ohio Medical Products. The 510(k) number is K833459.

When did COAXIAL VOL. VENTILATOR CIRCUIT receive FDA 510(k) clearance?

COAXIAL VOL. VENTILATOR CIRCUIT received FDA 510(k) clearance on 1984-01-10, under 510(k) number K833459.

Who is the listed applicant for COAXIAL VOL. VENTILATOR CIRCUIT?

The FDA 510(k) record lists Airco/Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAXIAL VOL. VENTILATOR CIRCUIT?

The FDA product code for COAXIAL VOL. VENTILATOR CIRCUIT is BZO.

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Other records listing Airco/Ohio Medical Products 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.

K833452OHIO GMS ABSORBERK832418OHIO TEMPERATURE SIMULATORK832565OHIO 5400 VOLUME MONITORK832185OHIO MODEL 922 SPIROMETERK830446OXYGEN MONITOR OHIO 5100K822456OHIO V5A ANESTHESIA VENTILATOR

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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