meddevicedb.com FDA Device Reference

NPAC

K936210 Class II Traditional
Decision Date
1994-02-03
Sponsor / Applicant
National Healthcare Linen Service

Technical Specification

510(k) Submission ID K936210
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1994-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NPAC received FDA 510(k) clearance under submission number K936210, sponsored by National Healthcare Linen Service. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1994-02-03.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.