meddevicedb.com FDA Device Reference

DULBECCO'S PHOSPHATE BUFFERED SALINE

K923652 Class II Traditional
Decision Date
1993-09-07
Sponsor / Applicant
Life-Tech Intl., Inc.

Technical Specification

510(k) Submission ID K923652
Product Code MFD
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5250
Decision Date 1993-09-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DULBECCO'S PHOSPHATE BUFFERED SALINE received FDA 510(k) clearance under submission number K923652, sponsored by Life-Tech Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1993-09-07.

Classification & Regulation

This clearance is catalogued under FDA product code MFD and 21 CFR 884.5250, within the Obstetrics/Gynecology review panel as a Class II device.