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

PRE-FILLED SYRINGE FOR KOALA IUP

K Number: K973746 · Decision Nov 24, 1997
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
8
Applicant Total
9
Review Days
54

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PRE-FILLED SYRINGE FOR KOALA IUP
K Number
K973746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2700
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clinical Innovations, Inc.
Date Received
October 1, 1997
Decision Date
November 24, 1997
Product Code
HFN
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HFN Transducer, Pressure, Intrauterine

Similar 510(k) Clearances

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

View all

Other Clearances by Clinical Innovations, Inc.

K Number Device Name
K030691 FETAL SPIRAL ELECTRODE, MODEL FSE07000
K022023 COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500
K003458 SOFT BEAT FETAL HEART RATE ELECTRODE MODEL SBT-7000
K981260 KIWI SOFT CUP WITH PALM PUMP MODEL NUMBER VFE-6000S, KIWI MUSHROOM CUP WITH PALM PUMP MODEL VFE-6000M
K974563 COLPO CUP CVC-2000
K974389 KOALA INTRAUTERINE PRESSURE CATHETER, KOALA EXTERNAL INTRAUTERINE PRESSURE CATHETER
K954955 STORC INTRAUTERINE PRESSURE CATHETER
K940681 CLEARVIEW UTERINE MANIPULATOR