Device Classification Name |
Mesh, Surgical
|
510(k) Number |
K983162 |
Device Name |
PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC |
Applicant |
BIO-VASCULAR, INC. |
2575 UNIVERSITY AVE. |
ST. PAUL,
MN
55114 -1024
|
|
Applicant Contact |
DIANNA L GECK |
Correspondent |
BIO-VASCULAR, INC. |
2575 UNIVERSITY AVE. |
ST. PAUL,
MN
55114 -1024
|
|
Correspondent Contact |
DIANNA L GECK |
Regulation Number | 878.3300
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 09/10/1998 |
Decision Date | 10/09/1998 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|