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FDA 510(k)

ENDOMED 433

K-Number: K823362 · 1983-03-09

ApplicantKipp & Zonen
Decision Date1983-03-09
Product Code
DecisionSubstantially Equivalent

Device Summary

ENDOMED 433 is the device name listed in this FDA 510(k) record. The listed applicant is Kipp & Zonen. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K823362. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOMED 433?

ENDOMED 433 is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Kipp & Zonen. The 510(k) number is K823362.

When did ENDOMED 433 receive FDA 510(k) clearance?

ENDOMED 433 received FDA 510(k) clearance on 1983-03-09, under 510(k) number K823362.

Who is the listed applicant for ENDOMED 433?

The FDA 510(k) record lists Kipp & Zonen as the applicant. This does not by itself establish the device manufacturer.

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.

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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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