The following data is part of a premarket notification filed by China National Medicines & Health Prod. I/e Corp. with the FDA for White Plume Absorbent Bandage.
| Device ID | K870315 |
| 510k Number | K870315 |
| Device Name: | WHITE PLUME ABSORBENT BANDAGE |
| Classification | 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products 510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la |
| Applicant | CHINA NATIONAL MEDICINES & HEALTH PROD. I/E CORP. C/O PACIFIC DEVELOPMENT GROUP 1000 T. JEFFERSON ST NW Suite 500, Washington, DC 20007 |
| Contact | Lisa Mitnick |
| Correspondent | Lisa Mitnick CHINA NATIONAL MEDICINES & HEALTH PROD. I/E CORP. C/O PACIFIC DEVELOPMENT GROUP 1000 T. JEFFERSON ST NW Suite 500, Washington, DC 20007 |
| Product Code | 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-28 |
| Decision Date | 1987-02-24 |