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

KENDALL CO2NFIRM NOW CO2 DETECTOR

K Number: K042572 · Decision Nov 5, 2004
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
12
Review Days
45

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Basic Information

Device Name
KENDALL CO2NFIRM NOW CO2 DETECTOR
K Number
K042572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kendall
Date Received
September 21, 2004
Decision Date
November 5, 2004
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNT), ordered by most recent decision date.

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Other Clearances by Kendall

K Number Device Name
K092797 ACUTE AND CHRONIC CATHETER REPAIR KIT
K062671 14.5 FR CHRONIC HEMODIALYSIS CATHETER WITH HEPARIN COATING AND SILVER IMPREGNATED SLEEVE (PALINDROME SAPPHIRE)
K060972 KEDALL 14.5 FR CHRONIC HEMODIALYSIS CATHETER W/SILVER IMPREGNATED SLEEVE (PALINDROME RUBY)
K053410 GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR
K051584 14.5 FR CHRONIC HEMODIALYSIS CATHETER WITH INSERTION STYLETS ACCESSORY
K043272 PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER WITH SLOTTED SYMMETRICAL TIP
K042461 KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304
K041914 PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER
K041006 TANDEM-CATH HEMODIALYSIS CATHETER, MODEL 10 FR
K040388 NEXT GENERATION SALEM SUMP
Search all 12 clearances from Kendall →