FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134

K Number: K981728 · Decision Jun 26, 1998
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
39
Review Days
42

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Basic Information

Device Name
ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134
K Number
K981728
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Alexander Mfg. Co.
Date Received
May 15, 1998
Decision Date
June 26, 1998
Product Code
BZQ
Advisory Committee
Anesthesiology
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
BZQ Monitor, Breathing Frequency

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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
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
K972787 ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M850-P
Search all 39 clearances from Alexander Mfg. Co. →