meddevicedb.com FDA Device Reference

HEYER-SCHULTE(R) 100CC & 400CC EXUDATE DISP. BAGS

K880650 Class I Traditional
Decision Date
1988-02-24
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K880650
Product Code GCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4680
Decision Date 1988-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEYER-SCHULTE(R) 100CC & 400CC EXUDATE DISP. BAGS received FDA 510(k) clearance under submission number K880650, sponsored by Baxter Healthcare Corp. 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 1988-02-24.

Classification & Regulation

This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.