Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DIA-KART

K-Number: K841180 · 1984-03-20

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

Device Summary

DIA-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 K841180. FDA Decision: Unknown.

Frequently Asked Questions

What is the DIA-KART?

DIA-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 K841180.

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

DIA-KART received FDA 510(k) clearance on 1984-03-20, under 510(k) number K841180.

Who is the listed applicant for DIA-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.

K841178ALU-KARTK841179HEMO-KART

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.

↑