PROBE & CATHETER— 510(k) K771663
Substantially EquivalentEdwards Laboratories
FDA 510(k) clearance K771663 for PROBE & CATHETER, Substantially Equivalent on 1977-09-20. Applicant: Edwards Laboratories. Device class: 2.
Clearance details
- Applicant
- Edwards Laboratories
- Product code
- Code KRB
- Device class
- Class 2
- Regulation
- 21 CFR 870.1915
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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- K991886 — PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSOR
More clearances from Edwards Laboratories
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