meddevicedb.com FDA Device Reference

PHOSPHATE BUFFERED SALINE (1X)

K811791 Class I Traditional
Decision Date
1981-08-25
Sponsor / Applicant
Dutchland Laboratories, Inc.

Technical Specification

510(k) Submission ID K811791
Product Code JCC
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1981-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHOSPHATE BUFFERED SALINE (1X) received FDA 510(k) clearance under submission number K811791, sponsored by Dutchland Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1981-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code JCC and 21 CFR 864.4010, within the Pathology review panel as a Class I device.