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

BAIM CORONARY SINUS FLOW ANALYZER

K Number: K811414 · Decision Jun 12, 1981
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
174
Applicant Total
35
Review Days
24

Basic Information

Device Name
BAIM CORONARY SINUS FLOW ANALYZER
K Number
K811414
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
ELECTRO-CATHETER CORP.
Date Received
May 19, 1981
Decision Date
June 12, 1981
Product Code
DXG
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
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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Other Clearances by ELECTRO-CATHETER CORP.

K Number Device Name
K934785 MULTIPACE
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K943257 TIP DEFLECTOR (GENESIS)
K933450 CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATION
K934787 SILICORE SEMI-FLOATER
K874154 ELECATH(R) TRANSESOPHAGEAL PACING CATHETER
K854511 ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SET
K854975 ELECATH PULSATILE PERFUSION PUMP
K850065 ELECATH TORKFLOAT PACING PROBE
K850324 ELECATH OPEN TIP BIPOLAR PACING CATHETER
Search all 35 clearances from ELECTRO-CATHETER CORP. →