EC-7701 FLUID WARMING CABINET

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

ENTHERMICS MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Enthermics Medical Systems, Inc. with the FDA for Ec-7701 Fluid Warming Cabinet.

Pre-market Notification Details

• Device ID: K993797
• 510k Number: K993797
• Device Name: EC-7701 FLUID WARMING CABINET
• 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: ENTHERMICS MEDICAL SYSTEMS, INC. 1900 K ST. NW Washington, DC 20006 -1108
• Contact: Emalee G Murphy
• Correspondent: Emalee G Murphy; ENTHERMICS MEDICAL SYSTEMS, INC. 1900 K ST. NW Washington, DC 20006 -1108
• Product Code: LDQ
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1999-11-09
• Decision Date: 2000-01-20
• Summary: summary