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STREPTOCOCCUS PNEUMONIAE CONTROL

K840512 Class I Traditional
Decision Date
1984-03-23
Sponsor / Applicant
Scientific Device Laboratory, Inc.

Technical Specification

510(k) Submission ID K840512
Product Code GTY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3740
Decision Date 1984-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STREPTOCOCCUS PNEUMONIAE CONTROL received FDA 510(k) clearance under submission number K840512, sponsored by Scientific Device Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1984-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code GTY and 21 CFR 866.3740, within the Microbiology review panel as a Class I device.