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FDA 510(k)

CYSTICERCOSIS SEROLOGICAL REAGENTS

K-Number: K900780 · 1990-10-04

ApplicantLmd Laboratories
Decision Date1990-10-04
Product CodeMDJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CYSTICERCOSIS SEROLOGICAL REAGENTS is the device name listed in this FDA 510(k) record. The listed applicant is Lmd Laboratories. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K900780. The device is classified under product code MDJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTICERCOSIS SEROLOGICAL REAGENTS?

CYSTICERCOSIS SEROLOGICAL REAGENTS is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Lmd Laboratories. The 510(k) number is K900780.

When did CYSTICERCOSIS SEROLOGICAL REAGENTS receive FDA 510(k) clearance?

CYSTICERCOSIS SEROLOGICAL REAGENTS received FDA 510(k) clearance on 1990-10-04, under 510(k) number K900780.

Who is the listed applicant for CYSTICERCOSIS SEROLOGICAL REAGENTS?

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 CYSTICERCOSIS SEROLOGICAL REAGENTS?

The FDA product code for CYSTICERCOSIS SEROLOGICAL REAGENTS is MDJ.

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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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