The following data is part of a premarket notification filed by American Edwards Laboratories with the FDA for Shear Force Gauge.
Device ID | K864330 |
510k Number | K864330 |
Device Name: | SHEAR FORCE GAUGE |
Classification | Catheter, Embolectomy |
Applicant | AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
Contact | Mark Cole |
Correspondent | Mark Cole AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
Product Code | DXE |
CFR Regulation Number | 870.5150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-11-04 |
Decision Date | 1987-01-06 |