The following data is part of a premarket notification filed by Site Microsurgical Systems, Inc. with the FDA for Site Diaphragm Cassette.
Device ID | K904186 |
510k Number | K904186 |
Device Name: | SITE DIAPHRAGM CASSETTE |
Classification | Device, Irrigation, Ocular Surgery |
Applicant | SITE MICROSURGICAL SYSTEMS, INC. 135 GIBRALTAR RD. Horsham, PA 19044 |
Contact | James K Mccracken |
Correspondent | James K Mccracken SITE MICROSURGICAL SYSTEMS, INC. 135 GIBRALTAR RD. Horsham, PA 19044 |
Product Code | KYG |
CFR Regulation Number | 886.4360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-09-12 |
Decision Date | 1990-11-21 |