meddevicedb.com FDA Device Reference

SPSMEDICAL SPORVIEW PA CULTURE SET

K081879 Class II Special
Decision Date
2008-07-30
Sponsor / Applicant
Spsmedical Supply Corp.

Technical Specification

510(k) Submission ID K081879
Product Code MRB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2008-07-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPSMEDICAL SPORVIEW PA CULTURE SET received FDA 510(k) clearance under submission number K081879, sponsored by Spsmedical Supply Corp.. 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 2008-07-30.

Classification & Regulation

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