ECG/RESPIRATION STIMULATOR— 510(k) K802205
Substantially EquivalentHealthdyne, Inc.
FDA 510(k) clearance K802205 for ECG/RESPIRATION STIMULATOR, Substantially Equivalent on 1980-10-03. Applicant: Healthdyne, Inc.. Device class: 2.
Clearance details
- Applicant
- Healthdyne, Inc.
- Product code
- Code BZQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.2375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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