The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Surgical Drapes.
| Device ID | K844802 |
| 510k Number | K844802 |
| Device Name: | SURGICAL DRAPES |
| Classification | Drape, Surgical |
| Applicant | PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
| Contact | James T O'reilly |
| Correspondent | James T O'reilly PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
| Product Code | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-12-11 |
| Decision Date | 1985-01-14 |