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ESP CULTURE SYSTEM - MYCO

K953129 Class I Traditional
Decision Date
1995-12-26
Sponsor / Applicant
Difco Laboratories, Inc.

Technical Specification

510(k) Submission ID K953129
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 1995-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ESP CULTURE SYSTEM - MYCO received FDA 510(k) clearance under submission number K953129, sponsored by Difco Laboratories, 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 1995-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code MDB and 21 CFR 866.2560, within the Microbiology review panel as a Class I device.