meddevicedb.com FDA Device Reference

GRASP (GRIGG-RUSSEL AIR SUPPORT PILLOW)

K901375 Class I Traditional
Decision Date
1990-04-19
Sponsor / Applicant
Medical Plastics Laboratory, Inc.

Technical Specification

510(k) Submission ID K901375
Product Code INW
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3750
Decision Date 1990-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRASP (GRIGG-RUSSEL AIR SUPPORT PILLOW) received FDA 510(k) clearance under submission number K901375, sponsored by Medical Plastics Laboratory, 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 1990-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code INW and 21 CFR 890.3750, within the Physical Medicine review panel as a Class I device.