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GOOD LUBRICATIONS

K020586 Class I Traditional
Decision Date
2003-01-24
Sponsor / Applicant
Biofilm, Inc.

Technical Specification

510(k) Submission ID K020586
Product Code KMJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6375
Decision Date 2003-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GOOD LUBRICATIONS received FDA 510(k) clearance under submission number K020586, sponsored by Biofilm, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2003-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code KMJ and 21 CFR 880.6375, within the General Hospital review panel as a Class I device.