The following data is part of a premarket notification filed by Dispomed, Inc. with the FDA for Non-sterile Gauze Sponge.
| Device ID | K891054 |
| 510k Number | K891054 |
| Device Name: | NON-STERILE GAUZE SPONGE |
| Classification | Absorber, Saliva, Paper |
| Applicant | DISPOMED, INC. 1201 SOUTH FLOWER ST. Burbank, CA 91520 |
| Contact | Kent Braniff |
| Correspondent | Kent Braniff DISPOMED, INC. 1201 SOUTH FLOWER ST. Burbank, CA 91520 |
| Product Code | KHR |
| CFR Regulation Number | 872.6050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-02-27 |
| Decision Date | 1989-05-01 |