The following data is part of a premarket notification filed by Cardinal Health, Inc. with the FDA for Laparoscopic Retractors.
| Device ID | K092684 |
| 510k Number | K092684 |
| Device Name: | LAPAROSCOPIC RETRACTORS |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | CARDINAL HEALTH, INC. 1430 WAUKEGAN ROAD- MPKB-3B Mcgaw Park, IL 60085 |
| Contact | Sharon Nichols |
| Correspondent | Sharon Nichols CARDINAL HEALTH, INC. 1430 WAUKEGAN ROAD- MPKB-3B Mcgaw Park, IL 60085 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-01 |
| Decision Date | 2010-01-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10885403156328 | K092684 | 000 |
| 10885403122750 | K092684 | 000 |
| 10885403122767 | K092684 | 000 |
| 10885403122774 | K092684 | 000 |
| 10885403122781 | K092684 | 000 |
| 10885403122798 | K092684 | 000 |
| 10885403122804 | K092684 | 000 |
| 10885403122811 | K092684 | 000 |
| 10885403122828 | K092684 | 000 |
| 10885403122835 | K092684 | 000 |
| 10885403122842 | K092684 | 000 |
| 10885403122859 | K092684 | 000 |
| 10885403122866 | K092684 | 000 |
| 10885403122873 | K092684 | 000 |
| 10885403122880 | K092684 | 000 |
| 70885403156931 | K092684 | 000 |