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FDA 510(k)

CART, EMERGENCY, CARDIOPULMONARY

K-Number: K872558 · 1987-07-24

Decision Date1987-07-24
Product CodeBZN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CART, EMERGENCY, CARDIOPULMONARY is the device name listed in this FDA 510(k) record. The listed applicant is Nico Metal Products Corp.. It received FDA 510(k) clearance on 1987-07-24 under 510(k) number K872558. The device is classified under product code BZN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CART, EMERGENCY, CARDIOPULMONARY?

CART, EMERGENCY, CARDIOPULMONARY is a medical device that received FDA 510(k) clearance on 1987-07-24. The listed applicant is Nico Metal Products Corp.. The 510(k) number is K872558.

When did CART, EMERGENCY, CARDIOPULMONARY receive FDA 510(k) clearance?

CART, EMERGENCY, CARDIOPULMONARY received FDA 510(k) clearance on 1987-07-24, under 510(k) number K872558.

Who is the listed applicant for CART, EMERGENCY, CARDIOPULMONARY?

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

What is the FDA product code for CART, EMERGENCY, CARDIOPULMONARY?

The FDA product code for CART, EMERGENCY, CARDIOPULMONARY is BZN.

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.

Related Devices (Code: BZN)

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.

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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