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S.S.T. SURGICAL THIMBLE

K895603 Class I Traditional
Decision Date
1989-10-06
Sponsor / Applicant
Healthcare Technologies Resources, Inc.

Technical Specification

510(k) Submission ID K895603
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1989-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S.S.T. SURGICAL THIMBLE received FDA 510(k) clearance under submission number K895603, sponsored by Healthcare Technologies Resources, 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 1989-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.