The following data is part of a premarket notification filed by U.s. Mfg. & Management, Inc. with the FDA for I.v. Start Kit, I.v. Restart Kit, Pedi-kit,geri-ki.
| Device ID | K853242 |
| 510k Number | K853242 |
| Device Name: | I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI |
| 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 | U.S. MFG. & MANAGEMENT, INC. 1802-F COMMERCENTER WEST San Bernardino, CA 92408 |
| Contact | Frank J Rauscher |
| Correspondent | Frank J Rauscher U.S. MFG. & MANAGEMENT, INC. 1802-F COMMERCENTER WEST San Bernardino, CA 92408 |
| 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 - With Drug (SESD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-08-01 |
| Decision Date | 1985-08-30 |