FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SEALED LEAD ACID BATTERY PACK

K Number: K970234 · Decision May 2, 1997
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
223
Applicant Total
18
Review Days
101

Basic Information

Device Name
SEALED LEAD ACID BATTERY PACK
K Number
K970234
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
PORTABLE POWER SYSTEMS, INC.
Date Received
January 21, 1997
Decision Date
May 2, 1997
Product Code
IZL
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IZL System, X-Ray, Mobile

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K931348 BATTERY PACK #1005NC
K933065 BATTERY PACK# S1009LA
K934015 RECHARGE REPLACE BATTERY PK SPACELABS 4045 MON/DEFIB
K934508 BATTERY PACK# S1024NC
K934439 RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITOR
K931484 REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S
K932823 BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK
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