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MEDSCAND DISPOSABLE PLASTIC VAGINAL SPECULUM; EASY-SPEC PLASTIC VAGINAL SPECULUM, MODEL 303

K984211 Class II Traditional
Decision Date
1998-12-23
Sponsor / Applicant
Medscand AB

Technical Specification

510(k) Submission ID K984211
Product Code HIB
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1998-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDSCAND DISPOSABLE PLASTIC VAGINAL SPECULUM; EASY-SPEC PLASTIC VAGINAL SPECULUM, MODEL 303 received FDA 510(k) clearance under submission number K984211, sponsored by Medscand AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1998-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code HIB and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.