Last synced on 21 February 2025 at 11:05 pm

Marker, Ostia, Aorto-Saphenous Vein

Page Type
Product Code
Regulation Medical Specialty
General and Plastic Surgery
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
878.4650
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code KPK is linked to regulation 21CFR878.4650, which does not seem to exist yet. It may be pending at the moment.

Marker, Ostia, Aorto-Saphenous Vein

Page Type
Product Code
Regulation Medical Specialty
General and Plastic Surgery
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
878.4650
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code KPK is linked to regulation 21CFR878.4650, which does not seem to exist yet. It may be pending at the moment.