The following data is part of a premarket notification filed by Peters Surgical with the FDA for Corolene.
| Device ID | K052701 |
| 510k Number | K052701 |
| Device Name: | COROLENE |
| Classification | Suture, Nonabsorbable, Synthetic, Polypropylene |
| Applicant | PETERS SURGICAL 42 RUE BENOIT FRANCHON Bobigny, FR 93013 |
| Contact | Annie Lasserre |
| Correspondent | Annie Lasserre PETERS SURGICAL 42 RUE BENOIT FRANCHON Bobigny, FR 93013 |
| Product Code | GAW |
| CFR Regulation Number | 878.5010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-09-28 |
| Decision Date | 2005-12-13 |
| Summary: | summary |