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FDA 510(k)

BENNETT VOLUME VENTILATOR CIRCUIT

K-Number: K812773 · 1981-10-23

ApplicantIdeal Medical, Inc.
Decision Date1981-10-23
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BENNETT VOLUME VENTILATOR CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Medical, Inc.. It received FDA 510(k) clearance on 1981-10-23 under 510(k) number K812773. 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 BENNETT VOLUME VENTILATOR CIRCUIT?

BENNETT VOLUME VENTILATOR CIRCUIT is a medical device that received FDA 510(k) clearance on 1981-10-23. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K812773.

When did BENNETT VOLUME VENTILATOR CIRCUIT receive FDA 510(k) clearance?

BENNETT VOLUME VENTILATOR CIRCUIT received FDA 510(k) clearance on 1981-10-23, under 510(k) number K812773.

Who is the listed applicant for BENNETT VOLUME VENTILATOR CIRCUIT?

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

What is the FDA product code for BENNETT VOLUME VENTILATOR CIRCUIT?

The FDA product code for BENNETT VOLUME VENTILATOR CIRCUIT is BZO.

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Other records listing Ideal Medical, Inc. 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.

K944067PEANUT WAND, MODIFICATIONK931115HATCHER STONE-EMBOLIS EXTRACTORK926335IDEAS PEANUT WANDK922161GRICE SOFT TISSUE BIOPSY KITK921922GRICE LAPAROSCOPIC SUTURING NEEDLEK915175REDDICK RETRACTOR

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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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