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SF REFEEDING MEDIA

K831685 Class I Traditional
Decision Date
1983-07-06
Sponsor / Applicant
Viromed Laboratories, Inc.

Technical Specification

510(k) Submission ID K831685
Product Code KIT
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.2220
Decision Date 1983-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SF REFEEDING MEDIA received FDA 510(k) clearance under submission number K831685, sponsored by Viromed Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1983-07-06.

Classification & Regulation

This clearance is catalogued under FDA product code KIT and 21 CFR 864.2220, within the Hematology review panel as a Class I device.