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

CARDIOPAC DEFIBRILLATOR 444

K Number: K844103 · Decision Jan 18, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
27
Review Days
87

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Basic Information

Device Name
CARDIOPAC DEFIBRILLATOR 444
K Number
K844103
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Birtcher Corp.
Date Received
October 23, 1984
Decision Date
January 18, 1985
Product Code
LDD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

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Other Clearances by Birtcher Corp.

K Number Device Name
K881328 MODEL 375 ECG
K860718 ELECTROSURGERY PENCIL, MODEL 767
K860687 BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768
K854814 SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33
K854864 BI-POLAR FORCEPS
K850668 ELECTROSURGICAL UNIT 774
K850943 MODEL 775 BIPOLAR COAGULATOR
K844101 CARDIO-NEC MODEL 365
K844104 CARDIO ANALYZER MODEL 380
K850297 ELECTROSURGICAL PENCIL HOLDER 720
Search all 27 clearances from Birtcher Corp. →