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ANTI-NATIVE DEOXYRIB-ONUCLEIC ACID ANTI

K790252 Class II Traditional
Decision Date
1979-03-15
Sponsor / Applicant
Meloy Laboratories, Inc.

Technical Specification

510(k) Submission ID K790252
Product Code DHN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1979-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTI-NATIVE DEOXYRIB-ONUCLEIC ACID ANTI received FDA 510(k) clearance under submission number K790252, sponsored by Meloy Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1979-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code DHN and 21 CFR 866.5100, within the Immunology review panel as a Class II device.