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PROVIDONE-IODINE SWABSTICKS

K830393 Class I Traditional
Decision Date
1983-04-06
Sponsor / Applicant
H & P Industries, Inc.

Technical Specification

510(k) Submission ID K830393
Product Code GEC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1983-04-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROVIDONE-IODINE SWABSTICKS received FDA 510(k) clearance under submission number K830393, sponsored by H & P Industries, Inc.. 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 1983-04-06.

Classification & Regulation

This clearance is catalogued under FDA product code GEC and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.