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

CURITY CENTRAL VENOUS CATHETER

K Number: K861829 · Decision Jul 10, 1986
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
63
Review Days
59

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Basic Information

Device Name
CURITY CENTRAL VENOUS CATHETER
K Number
K861829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
The Kendal Co.
Date Received
May 12, 1986
Decision Date
July 10, 1986
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

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Other Clearances by The Kendal Co.

K Number Device Name
K000087 MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
K990500 KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C
K991758 MONOJECT INSULIN SYRINGE
K970969 KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
K951488 KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
K942664 KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
K942774 POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING
K892434 KENDALL CURITY OXYGEN MASK
K892438 KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
K892440 KENDALL CURITY EXTENSION TUBES
Search all 63 clearances from The Kendal Co. →