FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

KENDALL CURITY OXYGEN NASAL CANNULA

K Number: K892435 · Decision Jun 12, 1989
Classifications
1
FEI Numbers
263
Registration Numbers
263
Same Product Code
41
Applicant Total
63
Review Days
63

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Basic Information

Device Name
KENDALL CURITY OXYGEN NASAL CANNULA
K Number
K892435
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5340
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
The Kendal Co.
Date Received
April 10, 1989
Decision Date
June 12, 1989
Product Code
CAT
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
CAT Cannula, Nasal, Oxygen

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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. →