meddevicedb.com FDA Device Reference

DISPOSE-A-SHEET

K933636 Class I Traditional
Decision Date
1994-01-26
Sponsor / Applicant
Belmac Healthcare Corp.

Technical Specification

510(k) Submission ID K933636
Product Code KME
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6060
Decision Date 1994-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSE-A-SHEET received FDA 510(k) clearance under submission number K933636, sponsored by Belmac Healthcare Corp.. 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 1994-01-26.

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.