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FDA 510(k)

ALU-KART

K-Number: K841178 · 1984-03-20

ApplicantMicro Encapsulation Tech.
Decision Date1984-03-20
Product Code
DecisionUnknown

Device Summary

ALU-KART is the device name listed in this FDA 510(k) record. The listed applicant is Micro Encapsulation Tech.. It received FDA 510(k) clearance on 1984-03-20 under 510(k) number K841178. FDA Decision: Unknown.

Frequently Asked Questions

What is the ALU-KART?

ALU-KART is a medical device that received FDA 510(k) clearance on 1984-03-20. The listed applicant is Micro Encapsulation Tech.. The 510(k) number is K841178.

When did ALU-KART receive FDA 510(k) clearance?

ALU-KART received FDA 510(k) clearance on 1984-03-20, under 510(k) number K841178.

Who is the listed applicant for ALU-KART?

The FDA 510(k) record lists Micro Encapsulation Tech. as the applicant. This does not by itself establish the device manufacturer.

Other records listing Micro Encapsulation Tech. 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.

K841180DIA-KARTK841179HEMO-KART

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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