FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ELECATH HEPARIN COATED THERMAL DILUTION

K Number: K832787 · Decision Oct 4, 1983
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
39
Applicant Total
35
Review Days
49

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Basic Information

Device Name
ELECATH HEPARIN COATED THERMAL DILUTION
K Number
K832787
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4360
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Electro-Catheter Corp.
Date Received
August 16, 1983
Decision Date
October 4, 1983
Product Code
KYG
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
KYG Device, Irrigation, Ocular Surgery

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K933451 OPEN 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
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