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DRESSING CHANGE KIT

K761192 Class I Traditional
Decision Date
1977-02-28
Sponsor / Applicant
Superior Plastic Products Corp.

Technical Specification

510(k) Submission ID K761192
Product Code JOK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6820
Decision Date 1977-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRESSING CHANGE KIT received FDA 510(k) clearance under submission number K761192, sponsored by Superior Plastic Products 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 1977-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code JOK and 21 CFR 880.6820, within the General Hospital review panel as a Class I device.