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CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST

K934193 Class II Traditional
Decision Date
1993-11-19
Sponsor / Applicant
Biosearch Medical Products, Inc.

Technical Specification

510(k) Submission ID K934193
Product Code EOX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4710
Decision Date 1993-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CELL-MATE(TM) MASS CYTOLOGY-CELLULAR RETRIEVAL SYST received FDA 510(k) clearance under submission number K934193, sponsored by Biosearch Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1993-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code EOX and 21 CFR 874.4710, within the Ear, Nose, Throat review panel as a Class II device.