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BATTERY PACK 1017LA

K931716 Class II Traditional
Decision Date
1994-02-07
Sponsor / Applicant
Portable Power Systems, Inc.

Technical Specification

510(k) Submission ID K931716
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1994-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BATTERY PACK 1017LA received FDA 510(k) clearance under submission number K931716, sponsored by Portable Power Systems, 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 1994-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.