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DRYASOL ACID CONCENTRATE MIX

K993212 Class II Special
Decision Date
1999-10-22
Sponsor / Applicant
Diasol, Inc.

Technical Specification

510(k) Submission ID K993212
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1999-10-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRYASOL ACID CONCENTRATE MIX received FDA 510(k) clearance under submission number K993212, sponsored by Diasol, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1999-10-22.

Classification & Regulation

This clearance is catalogued under FDA product code KPO and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.