The following data is part of a premarket notification filed by Peters Surgical with the FDA for Cardioflon, Cardioxyl.
| Device ID | K060163 |
| 510k Number | K060163 |
| Device Name: | CARDIOFLON, CARDIOXYL |
| Classification | Suture, Nonabsorbable, Synthetic, Polyethylene |
| Applicant | PETERS SURGICAL Z.I. LES VIGNES 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
| Contact | Annie Lasserre |
| Correspondent | Annie Lasserre PETERS SURGICAL Z.I. LES VIGNES 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
| Product Code | GAT |
| CFR Regulation Number | 878.5000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-23 |
| Decision Date | 2006-10-11 |
| Summary: | summary |