CART, EMERGENCY, CARDIOPULMONARY
K-Number: K872558 · 1987-07-24
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Device Summary
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
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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