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BAXTER AS40A, AS41 SYRINGE PUMP, MODEL N61WC

K012262 Class II Traditional
Decision Date
2001-09-12
Sponsor / Applicant
National Custom Ent., Inc.

Technical Specification

510(k) Submission ID K012262
Product Code MRZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2001-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAXTER AS40A, AS41 SYRINGE PUMP, MODEL N61WC received FDA 510(k) clearance under submission number K012262, sponsored by National Custom Ent., 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 2001-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code MRZ and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.