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

INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER

K Number: K970492 · Decision Apr 9, 1997
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
86
Applicant Total
42
Review Days
58

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Basic Information

Device Name
INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
K Number
K970492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ackrad Laboratories
Date Received
February 10, 1997
Decision Date
April 9, 1997
Product Code
LKF
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
LKF Cannula, Manipulator/Injector, Uterine

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

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Other Clearances by Ackrad Laboratories

K Number Device Name
K021272 SIB CATHETER, MODEL 61-7005
K020954 H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAY
K020951 H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007
K961752 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
K940176 ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION
K952542 ACKRAD ESOPHAGEAL BALLOON CATHETER SET
K953034 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
K915813 ACKRAD ERCP CONTRAST DELIVERY SET
K904499 NICOS (NON-INVASIVE CARDIAC OUTPUT SYSTEM)
K911780 INFANT NASAL CANNULAE ASSEMBLY, MODIFIED
Search all 42 clearances from Ackrad Laboratories →