CARDIOSERV P— 510(k) K962547
Substantially EquivalentMarquette Electronics, Inc.
FDA 510(k) clearance K962547 for CARDIOSERV P, Substantially Equivalent on 1997-03-06. 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.