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USCI PRESTO DISPOSABLE INFLATION DEVICE

K896415 Class II Traditional
Decision Date
1990-01-19
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K896415
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 1990-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

USCI PRESTO DISPOSABLE INFLATION DEVICE received FDA 510(k) clearance under submission number K896415, sponsored by C.R. Bard, 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 1990-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.