meddevicedb.com FDA Device Reference

SPORKS, PLASTIC, DISP.

K781191 Class I Traditional
Decision Date
1978-07-31
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K781191
Product Code ILC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 1978-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPORKS, PLASTIC, DISP. received FDA 510(k) clearance under submission number K781191, sponsored by Fred Sammons, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1978-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code ILC and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.