The following data is part of a premarket notification filed by Circuit Tree Medical, Inc. with the FDA for Ctm Reusable Pak.
| Device ID | K962430 |
| 510k Number | K962430 |
| Device Name: | CTM REUSABLE PAK |
| Classification | Unit, Phacofragmentation |
| Applicant | CIRCUIT TREE MEDICAL, INC. 9327 BLACKLEY ST. Temple City, CA 91780 -3139 |
| Contact | Glenn A Dunki-jacobs |
| Correspondent | Glenn A Dunki-jacobs CIRCUIT TREE MEDICAL, INC. 9327 BLACKLEY ST. Temple City, CA 91780 -3139 |
| Product Code | HQC |
| CFR Regulation Number | 886.4670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-24 |
| Decision Date | 1996-07-23 |