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RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB

K934015 Class II Traditional
Decision Date
1994-02-17
Sponsor / Applicant
Portable Power Systems, Inc.

Technical Specification

510(k) Submission ID K934015
Product Code LDD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5300
Decision Date 1994-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB received FDA 510(k) clearance under submission number K934015, 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 1994-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.