The following data is part of a premarket notification filed by Ansell Perry with the FDA for Sensi-derm Latex Surgical Gloves (powdered).
| Device ID | K980880 |
| 510k Number | K980880 |
| Device Name: | SENSI-DERM LATEX SURGICAL GLOVES (POWDERED) |
| Classification | Surgeon's Gloves |
| Applicant | ANSELL PERRY 1875 HARSH AVE. S.E. Massillon, OH 44646 -7199 |
| Contact | James R Chatterton |
| Correspondent | James R Chatterton ANSELL PERRY 1875 HARSH AVE. S.E. Massillon, OH 44646 -7199 |
| Product Code | KGO |
| CFR Regulation Number | 878.4460 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-03-09 |
| Decision Date | 1998-05-20 |
| Summary: | summary |