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

KENDALL CURITY CONTINUOUS EPIDDUAL ANESTHESIA CATH

K Number: K922113 · Decision Dec 3, 1992
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
74
Applicant Total
66
Review Days
212

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Basic Information

Device Name
KENDALL CURITY CONTINUOUS EPIDDUAL ANESTHESIA CATH
K Number
K922113
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5120
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health
Date Received
May 5, 1992
Decision Date
December 3, 1992
Product Code
BSO
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
BSO Catheter, Conduction, Anesthetic

Similar 510(k) Clearances

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Other Clearances by Kendall Healthcare Products Co. Div.Of Tyco Health

K Number Device Name
K973763 KENDALL CURITY IODOFORM PACKING STRIP
K973511 KENDALL CURITY PETROLATUM GAUZE
K973507 KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)
K973619 KENDALL CURITY NON-ADHERING DRESSING
K973509 KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING
K973546 KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
K970266 KENDALL HYDROPHILIC POWDER WOUND DRESSING
K963446 KENDALL DUAL LUMEN CATHETER
K964899 KENDALL CURITY URETERAL CATHETER
K964519 CURITY THORACENTESIS TRAY
Search all 66 clearances from Kendall Healthcare Products Co. Div.Of Tyco Health →