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TOWEL PACK

K952759 Class II Traditional
Decision Date
1995-09-29
Sponsor / Applicant
Medcare Custom Packaging, Inc.

Technical Specification

510(k) Submission ID K952759
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1995-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOWEL PACK received FDA 510(k) clearance under submission number K952759, sponsored by Medcare Custom Packaging, 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 1995-09-29.

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.