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FDA 510(k)

CARDIOPULMONARY METABOLIC MEASUEMENT CART

K-Number: K921565 · 1994-08-11

ApplicantQuiton Instrument Co.
Decision Date1994-08-11
Product CodeBZL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CARDIOPULMONARY METABOLIC MEASUEMENT CART is the device name listed in this FDA 510(k) record. The listed applicant is Quiton Instrument Co.. It received FDA 510(k) clearance on 1994-08-11 under 510(k) number K921565. The device is classified under product code BZL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOPULMONARY METABOLIC MEASUEMENT CART?

CARDIOPULMONARY METABOLIC MEASUEMENT CART is a medical device that received FDA 510(k) clearance on 1994-08-11. The listed applicant is Quiton Instrument Co.. The 510(k) number is K921565.

When did CARDIOPULMONARY METABOLIC MEASUEMENT CART receive FDA 510(k) clearance?

CARDIOPULMONARY METABOLIC MEASUEMENT CART received FDA 510(k) clearance on 1994-08-11, under 510(k) number K921565.

Who is the listed applicant for CARDIOPULMONARY METABOLIC MEASUEMENT CART?

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

What is the FDA product code for CARDIOPULMONARY METABOLIC MEASUEMENT CART?

The FDA product code for CARDIOPULMONARY METABOLIC MEASUEMENT CART is BZL.

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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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