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

PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15

K Number: K022752 · Decision Sep 9, 2003
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
30
Review Days
386

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Basic Information

Device Name
PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15
K Number
K022752
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hdc Corp.
Date Received
August 19, 2002
Decision Date
September 9, 2003
Product Code
CAZ
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
CAZ Anesthesia Conduction Kit

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K994059 CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07
K002770 IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL 700-08-10,700-08-11,700-08-12,700-08-15,700-08-16,735-08-10
K983119 ENTERO-TEST HP, MODEL #102-01
K983916 V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER)
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