510(k) K974352
- Device
- CARDIOVIEW 3000 SOFTWARE
- Applicant
- MICROMEDICAL, INC.
- 510(k) number
- K974352
- Product code
- LOS
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1998-09-08
- Date received
- 1997-11-19
- Regulation
- 510(k) Premarket Notification
- Classification name
- 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
- Medical specialty
- 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
- Review panel
- Cardiovascular
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- MALCOM CASTLE
- Address
- 255 Revere Dr., Suite 111 Northbrook IL US 60062 60062
FDA Registration Numbers#
- 8030978
- 3010381606
- 3003857828
- 3010082909
- 2433214
- 3031158
- 3003681187
- 1126271
- 1319390
- 3009443693
- 3007184699
Source Documents#
Legacy Summary#
summary
FDA Review#
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