meddevicedb.com FDA Device Reference

NEV'S INK AUTOCLAVE TAPES

K101580 Class II Traditional
Decision Date
2010-07-01
Sponsor / Applicant
Nev'S Ink, Inc.

Technical Specification

510(k) Submission ID K101580
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2010-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEV'S INK AUTOCLAVE TAPES received FDA 510(k) clearance under submission number K101580, sponsored by Nev'S Ink, 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 2010-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.