The following data is part of a premarket notification filed by Micromedical Industries, Ltd. with the FDA for Micromedical 12 Lead Simultaneous Cable.
| Device ID | K990266 |
| 510k Number | K990266 |
| Device Name: | MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE |
| 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 | MICROMEDICAL INDUSTRIES, LTD. 189 HAPP RD. Northfield, IL 60093 |
| Contact | Dean E Synder |
| Correspondent | Dean E Synder MICROMEDICAL INDUSTRIES, LTD. 189 HAPP RD. Northfield, IL 60093 |
| Product Code | LOS |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-01-28 |
| Decision Date | 1999-02-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00857175006166 | K990266 | 000 |
| 00857175006043 | K990266 | 000 |