Device Classification Name |
Laparoscope, Gynecologic (And Accessories)
|
510(k) Number |
K873115 |
Device Name |
CABOT FIBER LASER PROBE |
Applicant |
CABOT MEDICAL CORP. |
2021 CABOT BOULEVARD WEST |
LANGHORNE,
PA
19047
|
|
Applicant Contact |
JACK KELLER |
Correspondent |
CABOT MEDICAL CORP. |
2021 CABOT BOULEVARD WEST |
LANGHORNE,
PA
19047
|
|
Correspondent Contact |
JACK KELLER |
Regulation Number | 884.1720
|
Classification Product Code |
|
Date Received | 08/10/1987 |
Decision Date | 01/28/1988 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Obstetrics/Gynecology
|
510k Review Panel |
Obstetrics/Gynecology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|