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KOALA INTRAUTERINE PRESSURE CATHETER, KOALA EXTERNAL INTRAUTERINE PRESSURE CATHETER

FDA 510(k) clearance K974389 · decided 1998-02-19

Clearance details

K-number
K974389
Device name
KOALA INTRAUTERINE PRESSURE CATHETER, KOALA EXTERNAL INTRAUTERINE PRESSURE CATHETER
Applicant
Clinical Innovations, Inc.
Decision
Substantially Equivalent
Date received
1997-11-21
Decision date
1998-02-19
Days to decision
90 days
Clearance type
Traditional
Product code
HFN
Device class
2
Regulation number
884.2700
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Murray, UT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Koala Intrauterine Pressure Catheter (IPC-5000E) (K250897)Clinical Innovations, LLC2025-05-22
PRE-FILLED SYRINGE FOR KOALA IUP (K973746)Clinical Innovations, Inc.1997-11-24
INTRAN 500 (K961424)Utah Medical Products, Inc.1996-07-10
STORC INTRAUTERINE PRESSURE CATHETER (K954955)Clinical Innovations, Inc.1996-04-17
INTRAN PLUS (K955443)Utah Medical Products, Inc.1996-02-20
DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER (K920375)Telos Medical Corp.1992-10-27
ULTRANS DISPOSABLE INTRAUTERINE (K882224)Telos Medical Corp.1989-10-12
SOFSENS(TM) MODEL LMP-100 INTRAUTERINE PRES. TRANS (K893503)Laurel Medical Corp.1989-06-12

Recalls involving this device

No recalls on record reference this clearance.