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LSVP INTERNATIONAL BIOPSY FORCEPS

K982983 Class II Traditional
Decision Date
1998-09-29
Sponsor / Applicant
Lsvp Intl., Inc.

Technical Specification

510(k) Submission ID K982983
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 1998-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LSVP INTERNATIONAL BIOPSY FORCEPS received FDA 510(k) clearance under submission number K982983, sponsored by Lsvp Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1998-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.