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

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL9366

K Number: K972786 · Decision Oct 17, 1997
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
39
Review Days
84

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Basic Information

Device Name
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL9366
K Number
K972786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Alexander Mfg. Co.
Date Received
July 25, 1997
Decision Date
October 17, 1997
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

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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
K972780 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL625
K972779 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS3030-P
Search all 39 clearances from Alexander Mfg. Co. →