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C2 MEDICAL GLOVES

K113639 Class I Traditional
Decision Date
2012-05-08
Sponsor / Applicant
Amercare, Inc.

Technical Specification

510(k) Submission ID K113639
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2012-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C2 MEDICAL GLOVES received FDA 510(k) clearance under submission number K113639, sponsored by Amercare, 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 2012-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.