The following data is part of a premarket notification filed by Moore Medical Corp. with the FDA for Patient Examination Gloves (latex).
| Device ID | K892470 |
| 510k Number | K892470 |
| Device Name: | PATIENT EXAMINATION GLOVES (LATEX) |
| Classification | Latex Patient Examination Glove |
| Applicant | MOORE MEDICAL CORP. 80 LEBUH RAYA KAPAL OFF JALAN CHAIN FERRY, 12100 Butterworth, Penang., MY |
| Contact | Kheng Liat |
| Correspondent | Kheng Liat MOORE MEDICAL CORP. 80 LEBUH RAYA KAPAL OFF JALAN CHAIN FERRY, 12100 Butterworth, Penang., MY |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-07 |
| Decision Date | 1989-07-14 |