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DISPOSABLE PILLOW

K842336 Class I Traditional
Decision Date
1984-07-13
Sponsor / Applicant
Monterey Mills, Inc.

Technical Specification

510(k) Submission ID K842336
Product Code KME
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6060
Decision Date 1984-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE PILLOW received FDA 510(k) clearance under submission number K842336, sponsored by Monterey Mills, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1984-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code KME and 21 CFR 880.6060, within the General Hospital review panel as a Class I device.