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FDA 510(k)

OPERATING ROOM VENTILATOR

K-Number: K770084 · 1977-02-23

ApplicantDupaco, Inc.
Decision Date1977-02-23
Product CodeFZH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATING ROOM VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dupaco, Inc.. It received FDA 510(k) clearance on 1977-02-23 under 510(k) number K770084. The device is classified under product code FZH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING ROOM VENTILATOR?

OPERATING ROOM VENTILATOR is a medical device that received FDA 510(k) clearance on 1977-02-23. The listed applicant is Dupaco, Inc.. The 510(k) number is K770084.

When did OPERATING ROOM VENTILATOR receive FDA 510(k) clearance?

OPERATING ROOM VENTILATOR received FDA 510(k) clearance on 1977-02-23, under 510(k) number K770084.

Who is the listed applicant for OPERATING ROOM VENTILATOR?

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

What is the FDA product code for OPERATING ROOM VENTILATOR?

The FDA product code for OPERATING ROOM VENTILATOR is FZH.

Related Clinical Trials

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Other records listing Dupaco, 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.

K841581UNIFILTER ANESTHESIA & RESPIRATORY FILTK830395PEEPERK821434EKG (ECG) ELECTRODES

Related Devices (Code: FZH)

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.

K923233CARDIO-PAK LAPAROTOMY PACKCardio-Med-Associates, Inc.K875305MODEL UCA / SPEC SYSTEM UCASpec Systems, Inc.K871901ULTRAFLOWCustom Industries, 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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