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PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS

K992476 Class I Traditional
Decision Date
2000-09-13
Sponsor / Applicant
Pilling Weck Surgical

Technical Specification

510(k) Submission ID K992476
Product Code MWS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4500
Decision Date 2000-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS received FDA 510(k) clearance under submission number K992476, sponsored by Pilling Weck Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code MWS and 21 CFR 870.4500, within the Cardiovascular review panel as a Class I device.