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FDA 510(k)

MR1 LUTROPIN RIA KIT

K-Number: K820741 · 1982-04-14

ApplicantMicroanalytic Research, Inc.
Decision Date1982-04-14
Product CodeCEP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MR1 LUTROPIN RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Microanalytic Research, Inc.. It received FDA 510(k) clearance on 1982-04-14 under 510(k) number K820741. The device is classified under product code CEP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR1 LUTROPIN RIA KIT?

MR1 LUTROPIN RIA KIT is a medical device that received FDA 510(k) clearance on 1982-04-14. The listed applicant is Microanalytic Research, Inc.. The 510(k) number is K820741.

When did MR1 LUTROPIN RIA KIT receive FDA 510(k) clearance?

MR1 LUTROPIN RIA KIT received FDA 510(k) clearance on 1982-04-14, under 510(k) number K820741.

Who is the listed applicant for MR1 LUTROPIN RIA KIT?

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

What is the FDA product code for MR1 LUTROPIN RIA KIT?

The FDA product code for MR1 LUTROPIN RIA KIT is CEP.

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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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