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BLOOD PRESSURE CUFF 1

K951039 Class II Traditional
Decision Date
1995-10-31
Sponsor / Applicant
Pedia Pals, Inc.

Technical Specification

510(k) Submission ID K951039
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 1995-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD PRESSURE CUFF 1 received FDA 510(k) clearance under submission number K951039, sponsored by Pedia Pals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1995-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.