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FDA 510(k)

CART

K-Number: K823925 · 1983-03-28

ApplicantMedical Assoc. Intl., Inc.
Decision Date1983-03-28
Product Code
DecisionSubstantially Equivalent

Device Summary

CART is the device name listed in this FDA 510(k) record. The listed applicant is Medical Assoc. Intl., Inc.. It received FDA 510(k) clearance on 1983-03-28 under 510(k) number K823925. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CART?

CART is a medical device that received FDA 510(k) clearance on 1983-03-28. The listed applicant is Medical Assoc. Intl., Inc.. The 510(k) number is K823925.

When did CART receive FDA 510(k) clearance?

CART received FDA 510(k) clearance on 1983-03-28, under 510(k) number K823925.

Who is the listed applicant for CART?

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

Other records listing Medical Assoc. Intl., 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.

K853347MAI STERILE UTILITY DRAPE

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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