AMPLIFIER MODULE, 78211A ECG— 510(k) K772132
Substantially EquivalentHewlett-Packard Co.
FDA 510(k) clearance K772132 for AMPLIFIER MODULE, 78211A ECG, Substantially Equivalent on 1977-11-22. Applicant: Hewlett-Packard Co.. Device class: 2.
Clearance details
- Applicant
- Hewlett-Packard Co.
- Product code
- Code DRR
- Device class
- Class 2
- Regulation
- 21 CFR 870.2050
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.