FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ACKRAD H/S PROCEDURE TRAY

K Number: K881680 · Decision Jul 15, 1988
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
55
Applicant Total
42
Review Days
87

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Basic Information

Device Name
ACKRAD H/S PROCEDURE TRAY
K Number
K881680
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1700
Medical Specialty
Obstetrics/Gynecology
Decision
Unknown
Applicant
Ackrad Laboratories
Date Received
April 19, 1988
Decision Date
July 15, 1988
Product Code
HIG
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
HIG Insufflator, Hysteroscopic

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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
K970492 INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
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)
Search all 42 clearances from Ackrad Laboratories →