The following data is part of a premarket notification filed by Johnson & Johnson Medical, Inc. with the FDA for Latex Medical Glove.
| Device ID | K943900 |
| 510k Number | K943900 |
| Device Name: | LATEX MEDICAL GLOVE |
| Classification | Latex Patient Examination Glove |
| Applicant | JOHNSON & JOHNSON MEDICAL, INC. 2500 ARBROOK BLVD. P.O.BOX 90130 Arlington, TX 76004 -0130 |
| Contact | Ralph H Larsen |
| Correspondent | Ralph H Larsen JOHNSON & JOHNSON MEDICAL, INC. 2500 ARBROOK BLVD. P.O.BOX 90130 Arlington, TX 76004 -0130 |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-10 |
| Decision Date | 1994-12-12 |