The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kimberly-clark Procedure Gown.
| Device ID | K052824 |
| 510k Number | K052824 |
| Device Name: | KIMBERLY-CLARK PROCEDURE GOWN |
| Classification | Gown, Surgical |
| Applicant | KIMBERLY-CLARK CORP. 1400 HOLCOMB BRIDGE RD. Roswell, GA 30076 |
| Contact | Cheryl M Sanzare |
| Correspondent | Cheryl M Sanzare KIMBERLY-CLARK CORP. 1400 HOLCOMB BRIDGE RD. Roswell, GA 30076 |
| Product Code | FYA |
| CFR Regulation Number | 878.4040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-10-05 |
| Decision Date | 2006-05-02 |
| Summary: | summary |