Device Classification Name |
forceps, biopsy, electric
|
510(k) Number |
K905088 |
Device Name |
HOT BIOPSY FORCEPS |
Applicant |
ESCO PRECISION, INC. |
21 WILLIAM PENN DR. |
STONY BROOK,
NY
11790
|
|
Applicant Contact |
TED ESSER |
Correspondent |
ESCO PRECISION, INC. |
21 WILLIAM PENN DR. |
STONY BROOK,
NY
11790
|
|
Correspondent Contact |
TED ESSER |
Regulation Number | 876.4300
|
Classification Product Code |
|
Date Received | 11/14/1990 |
Decision Date | 03/19/1991 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|