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

TRIP TONOMETRY CATHETER, 16F

K Number: K983366 · Decision Dec 23, 1998
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
9
Review Days
90

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Basic Information

Device Name
TRIP TONOMETRY CATHETER, 16F
K Number
K983366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Datex-Engstrom, Inc.
Date Received
September 24, 1998
Decision Date
December 23, 1998
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

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Other Clearances by Datex-Engstrom, Inc.

K Number Device Name
K982091 CS/3 COMPACT AIRWAY MODULE, M-COVX
K981378 DATEX-ENGSTROM LIGHT MONITOR MODELS F-LM1, F-LMP1
K973985 AS/3 ANAESTHESIA DELIVERY UNIT (AS/3 ADU)
K980362 MRI COMPATIBLE MONITOR AND ACCESSORIES
K974792 CS/3(TM) MONITORS*
K980384 TRIP TONOMETRY CATHETER, 18F
K974747 CS/3 ARRHYTHMIA WORKSTATION
K974101 DATEX-ENGSTROM NETWORK