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

LOPER CELIAC PLEXUS BLOCK CATHETER KIT

K Number: K895955 · Decision Feb 22, 1990
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
7
Review Days
134

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Basic Information

Device Name
LOPER CELIAC PLEXUS BLOCK CATHETER KIT
K Number
K895955
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Opticon Medical, Inc.
Date Received
October 11, 1989
Decision Date
February 22, 1990
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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K023090 OPTION-VF URINARY CATHETER, FV14218
K970716 OPTICON DIRECT MALE URINARY CATHETER FOR CONTINUOUS DRAINAGE
K930194 HEMOSTASIS VALVE AND TUBING SET
K904999 WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE
K895476 OPTION EPIDURAL CATHETERS