CHEST FLUID MONITOR— 510(k) K772092
Substantially EquivalentDynatech Research & Development Co.
FDA 510(k) clearance K772092 for CHEST FLUID MONITOR, Substantially Equivalent on 1977-11-18. Applicant: Dynatech Research & Development Co.. Device class: 2.
Clearance details
- Applicant
- Dynatech Research & Development Co.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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