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SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES

K801070 Class II Traditional
Decision Date
1980-07-21
Sponsor / Applicant
Sherwood Medical Industries

Technical Specification

510(k) Submission ID K801070
Product Code HHK
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1175
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES received FDA 510(k) clearance under submission number K801070, sponsored by Sherwood Medical Industries. 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 1980-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code HHK and 21 CFR 884.1175, within the Obstetrics/Gynecology review panel as a Class II device.