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FDA 510(k)

TRICHINELLA SEROLOGY MICROTITER ELISA

K-Number: K904613 · 1991-03-21

ApplicantLmd Laboratories
Decision Date1991-03-21
Product CodeGPG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRICHINELLA SEROLOGY MICROTITER ELISA is the device name listed in this FDA 510(k) record. The listed applicant is Lmd Laboratories. It received FDA 510(k) clearance on 1991-03-21 under 510(k) number K904613. The device is classified under product code GPG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRICHINELLA SEROLOGY MICROTITER ELISA?

TRICHINELLA SEROLOGY MICROTITER ELISA is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is Lmd Laboratories. The 510(k) number is K904613.

When did TRICHINELLA SEROLOGY MICROTITER ELISA receive FDA 510(k) clearance?

TRICHINELLA SEROLOGY MICROTITER ELISA received FDA 510(k) clearance on 1991-03-21, under 510(k) number K904613.

Who is the listed applicant for TRICHINELLA SEROLOGY MICROTITER ELISA?

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

What is the FDA product code for TRICHINELLA SEROLOGY MICROTITER ELISA?

The FDA product code for TRICHINELLA SEROLOGY MICROTITER ELISA is GPG.

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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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