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CARAPACE LABOR AND DELIVERY SETS

K931722 Class II Traditional
Decision Date
1994-03-23
Sponsor / Applicant
Carapace, Inc.

Technical Specification

510(k) Submission ID K931722
Product Code MLS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1994-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARAPACE LABOR AND DELIVERY SETS received FDA 510(k) clearance under submission number K931722, sponsored by Carapace, Inc.. 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 1994-03-23.

Classification & Regulation

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