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DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC

K930775 Class I Traditional
Decision Date
1993-04-23
Sponsor / Applicant
Falcon Instruments, Inc.

Technical Specification

510(k) Submission ID K930775
Product Code MDM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1993-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC received FDA 510(k) clearance under submission number K930775, sponsored by Falcon Instruments, 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 1993-04-23.

Classification & Regulation

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