meddevicedb.com FDA Device Reference

DEROYAL SURGICAL (SURGIMATE) PENCIL ADAPTERS

K961087 Class II Traditional
Decision Date
1996-05-16
Sponsor / Applicant
Debusk Knitting Mills, Div. Deroyal Industries

Technical Specification

510(k) Submission ID K961087
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1996-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEROYAL SURGICAL (SURGIMATE) PENCIL ADAPTERS received FDA 510(k) clearance under submission number K961087, sponsored by Debusk Knitting Mills, Div. Deroyal Industries. 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 1996-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.