PREAMPLIFIER MODULE, EKG RESPIRATION— 510(k) K790304
Substantially EquivalentAbbott Medical Electronics Co.
FDA 510(k) clearance K790304 for PREAMPLIFIER MODULE, EKG RESPIRATION, Substantially Equivalent on 1979-02-27. Applicant: Abbott Medical Electronics Co..
Clearance details
- Applicant
- Abbott Medical Electronics Co.
- Product code
- Code BZQ
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fort Worth, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.