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FDA 510(k)

VENTILATORY FREQUENCY MONITOR

K-Number: K834569 · 1984-03-30

ApplicantCryo Corp.
Decision Date1984-03-30
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATORY FREQUENCY MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Cryo Corp.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K834569. 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 VENTILATORY FREQUENCY MONITOR?

VENTILATORY FREQUENCY MONITOR is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Cryo Corp.. The 510(k) number is K834569.

When did VENTILATORY FREQUENCY MONITOR receive FDA 510(k) clearance?

VENTILATORY FREQUENCY MONITOR received FDA 510(k) clearance on 1984-03-30, under 510(k) number K834569.

Who is the listed applicant for VENTILATORY FREQUENCY MONITOR?

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

What is the FDA product code for VENTILATORY FREQUENCY MONITOR?

The FDA product code for VENTILATORY FREQUENCY MONITOR is BZO.

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 Cryo Corp. 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.

K872145CELLSOFT(TM)-CASA (SERIES 1000,2000 & 3000)K833994PULSAIR I & II

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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