MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE

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

MICROMEDICAL INDUSTRIES, LTD.

The following data is part of a premarket notification filed by Micromedical Industries, Ltd. with the FDA for Micromedical 12 Lead Simultaneous Cable.

Pre-market Notification Details

• 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

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00857175006166	K990266	000
00857175006043	K990266	000