The following data is part of a premarket notification filed by Encore Technology, Inc. with the FDA for Patient Examination Gloves (latex).
| Device ID | K891425 |
| 510k Number | K891425 |
| Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
| Classification | Latex Patient Examination Glove |
| Applicant | ENCORE TECHNOLOGY, INC. 4655 OLD IRONSIDES DRIVE, #215 Santa Clara, CA 95050 |
| Contact | Fred Kinder |
| Correspondent | Fred Kinder ENCORE TECHNOLOGY, INC. 4655 OLD IRONSIDES DRIVE, #215 Santa Clara, CA 95050 |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-03-14 |
| Decision Date | 1989-03-29 |