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

CADD MEDICATION CASSETTE RESERVOIR

K Number: K081156 · Decision Jul 18, 2008
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
20
Review Days
86

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Basic Information

Device Name
CADD MEDICATION CASSETTE RESERVOIR
K Number
K081156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smiths Medical MD, Inc.
Date Received
April 23, 2008
Decision Date
July 18, 2008
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

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K Number Device Name
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K101180 GRIPPER MICRO BLUNT CANNULA, NON-CORING SAFETY NEEDLE (GRIPPER MICRO NEEDLE) MODEL: 21-3253-24, 21-3258-24, 21-3262-24,
K091181 LOCKBOX FOR USE WITH MEDFUSION 3000 SERIES PUMPS
K082783 CADD -SOLIS MEDICATION SAFETY SOFTWARE: ADMINISTRATOR AND POINT-OF-CARE
K080743 LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP
K072144 CADD -SOLIS AMBULATORY INFUSION PUMP AND CADD -SOLIS MEDICATION SAFETY SOFTWARE - ADMINISTRATOR
K072955 CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE-ADMINISTRATOR (21-6275), POINT OF CARE (21-6276)
K072657 POWER PORT-A-CATH, CATH II, AND P.A.S. PORT T2 POWER P.A.C. IMPLANTABLE VENOUS ACCESS SYSTEMS AND POWER GRIPPER PLUS
K072059 GRIPPER MICRO NEEDLE
Search all 20 clearances from Smiths Medical MD, Inc. →