RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM— 510(k) K963120
Substantially EquivalentMarquette Electronics, Inc.
FDA 510(k) clearance K963120 for RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM, Substantially Equivalent on 1997-02-28. Applicant: Marquette Electronics, Inc.. Device class: 2.
Clearance details
- Applicant
- Marquette Electronics, Inc.
- Product code
- Code DRO
- Device class
- Class 2
- Regulation
- 21 CFR 870.5550
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milwaukee, WI, US
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More clearances from Marquette Electronics, Inc.
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