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FDA 510(k)

CIRCUIT, INTENSIVE CARE VENTILATOR

K-Number: K760352 · 1976-08-11

ApplicantMonaghan Medical Corp.
Decision Date1976-08-11
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRCUIT, INTENSIVE CARE VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760352. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUIT, INTENSIVE CARE VENTILATOR?

CIRCUIT, INTENSIVE CARE VENTILATOR is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K760352.

When did CIRCUIT, INTENSIVE CARE VENTILATOR receive FDA 510(k) clearance?

CIRCUIT, INTENSIVE CARE VENTILATOR received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760352.

Who is the listed applicant for CIRCUIT, INTENSIVE CARE VENTILATOR?

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

What is the FDA product code for CIRCUIT, INTENSIVE CARE VENTILATOR?

The FDA product code for CIRCUIT, INTENSIVE CARE VENTILATOR is CAZ.

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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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