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AQUAGEL LUBRICATING JELLY

K951431 Class I Traditional
Decision Date
1995-07-21
Sponsor / Applicant
Depuy Healthcare

Technical Specification

510(k) Submission ID K951431
Product Code KMJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6375
Decision Date 1995-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQUAGEL LUBRICATING JELLY received FDA 510(k) clearance under submission number K951431, sponsored by Depuy Healthcare. 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 1995-07-21.

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.