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ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT

K080202 Class II Special
Decision Date
2008-05-08
Sponsor / Applicant
Oncobionics, Inc.

Technical Specification

510(k) Submission ID K080202
Product Code OAB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2008-05-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT received FDA 510(k) clearance under submission number K080202, sponsored by Oncobionics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2008-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code OAB and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.