FDA 510(k) Substantially Equivalent 🇺🇸 United States

ACKRAD SIALOGRAPHY CATHETER

K Number: K852154 · Decision Jun 26, 1985
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
42
Review Days
40

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Basic Information

Device Name
ACKRAD SIALOGRAPHY CATHETER
K Number
K852154
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Ackrad Laboratories
Date Received
May 17, 1985
Decision Date
June 26, 1985
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

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 →