The following data is part of a premarket notification filed by Site Microsurgical Systems, Inc. with the FDA for Site Ultrasonic I/a Phaco Needle.
Device ID | K882103 |
510k Number | K882103 |
Device Name: | SITE ULTRASONIC I/A PHACO NEEDLE |
Classification | Unit, Phacofragmentation |
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 | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-05-19 |
Decision Date | 1988-07-01 |