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COLONGLIDE LUBRICANT

K141028 Class I Special
Decision Date
2014-07-24
Sponsor / Applicant
Pediatric Pharmaceuticals, Inc.

Technical Specification

510(k) Submission ID K141028
Product Code KMJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6375
Decision Date 2014-07-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COLONGLIDE LUBRICANT received FDA 510(k) clearance under submission number K141028, sponsored by Pediatric Pharmaceuticals, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2014-07-24.

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.