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ACE CUSTOM SURGICAL PACK

K922648 Class II Traditional
Decision Date
1993-03-20
Sponsor / Applicant
Ace Surgical Supply Co., Inc.

Technical Specification

510(k) Submission ID K922648
Product Code LRO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1993-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE CUSTOM SURGICAL PACK received FDA 510(k) clearance under submission number K922648, sponsored by Ace Surgical Supply Co., 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 1993-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code LRO and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.