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FDA 510(k)

END TIDAL CO2 ANALYZER #411

K-Number: K830253 · 1983-03-31

Decision Date1983-03-31
Product Code
DecisionSubstantially Equivalent

Device Summary

END TIDAL CO2 ANALYZER #411 is the device name listed in this FDA 510(k) record. The listed applicant is Andros Incorporated. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830253. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the END TIDAL CO2 ANALYZER #411?

END TIDAL CO2 ANALYZER #411 is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Andros Incorporated. The 510(k) number is K830253.

When did END TIDAL CO2 ANALYZER #411 receive FDA 510(k) clearance?

END TIDAL CO2 ANALYZER #411 received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830253.

Who is the listed applicant for END TIDAL CO2 ANALYZER #411?

The FDA 510(k) record lists Andros Incorporated 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.

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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