The following data is part of a premarket notification filed by American Edwards Laboratories with the FDA for American Edwards 4.0 Mm Arthroscope.
Device ID | K863597 |
510k Number | K863597 |
Device Name: | AMERICAN EDWARDS 4.0 MM ARTHROSCOPE |
Classification | Arthroscope |
Applicant | AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
Contact | Dieck, Phd |
Correspondent | Dieck, Phd AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
Product Code | HRX |
CFR Regulation Number | 888.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-09-15 |
Decision Date | 1986-09-25 |