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

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P

K Number: K971213 · Decision May 27, 1997
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
47
Applicant Total
39
Review Days
55

Basic Information

Device Name
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P
K Number
K971213
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ALEXANDER MFG. CO.
Date Received
April 2, 1997
Decision Date
May 27, 1997
Product Code
MRZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
MRZ Accessories, Pump, Infusion

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Other Clearances by ALEXANDER MFG. CO.

K Number Device Name
K982896 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP9
K981776 ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146X
K981728 ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134
K980224 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822
K974061 RECHARGEABLE BATTERY PART NUMBER GL825-200
K973851 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630
K973850 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M007
K972746 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP6/100
K972779 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS3030-P
K972780 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL625
Search all 39 clearances from ALEXANDER MFG. CO. →