The following data is part of a premarket notification filed by I.c. Medical, Inc. with the FDA for Crystal Vision And Accessories.
| Device ID | K932230 |
| 510k Number | K932230 |
| Device Name: | CRYSTAL VISION AND ACCESSORIES |
| Classification | Apparatus, Exhaust, Surgical |
| Applicant | I.C. MEDICAL, INC. 2340 W. SHANGRI LA SUITE 202 Phoenix, AZ 85029 |
| Contact | Kurt Hasper |
| Correspondent | Kurt Hasper I.C. MEDICAL, INC. 2340 W. SHANGRI LA SUITE 202 Phoenix, AZ 85029 |
| Product Code | FYD |
| CFR Regulation Number | 878.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-07 |
| Decision Date | 1994-02-18 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817688022411 | K932230 | 000 |
| 00817688021711 | K932230 | 000 |
| 00817688021704 | K932230 | 000 |
| 00817688021698 | K932230 | 000 |
| 00817688021681 | K932230 | 000 |
| 00817688021667 | K932230 | 000 |
| 00817688021643 | K932230 | 000 |
| 00817688021629 | K932230 | 000 |
| 00817688021605 | K932230 | 000 |
| 00817688021582 | K932230 | 000 |
| 00817688021544 | K932230 | 000 |
| 00817688021520 | K932230 | 000 |
| 00817688021506 | K932230 | 000 |
| 00817688021483 | K932230 | 000 |
| 00817688021469 | K932230 | 000 |
| 00817688021742 | K932230 | 000 |
| 00817688021759 | K932230 | 000 |
| 00817688022381 | K932230 | 000 |
| 00817688022374 | K932230 | 000 |
| 00817688022367 | K932230 | 000 |
| 00817688022350 | K932230 | 000 |
| 00817688021957 | K932230 | 000 |
| 00817688021872 | K932230 | 000 |
| 00817688021865 | K932230 | 000 |
| 00817688021858 | K932230 | 000 |
| 00817688021841 | K932230 | 000 |
| 00817688021834 | K932230 | 000 |
| 00817688021827 | K932230 | 000 |
| 00817688021810 | K932230 | 000 |
| 00817688021797 | K932230 | 000 |
| 00817688021780 | K932230 | 000 |
| 00817688021445 | K932230 | 000 |