510(k) K895683

BERNARD VESSEL APPROXIMATOR by Applied Medical Technologies — Product Code HRQ

K895683 is an FDA 510(k) premarket notification submitted by Applied Medical Technologies for the device "BERNARD VESSEL APPROXIMATOR". The FDA issued a decision of Substantially Equivalent on October 24, 1989. The device falls under product code HRQ (Hemostat), a Class I device regulated under 21 CFR 878.4800. Applied Medical Technologies has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 1989
Date Received
September 21, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hemostat
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type