ACUITY CENTRAL STATION— 510(k) K972121
Substantially EquivalentProtocol Systems, Inc.
FDA 510(k) clearance K972121 for ACUITY CENTRAL STATION, Substantially Equivalent on 1997-11-07. Applicant: Protocol Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Protocol Systems, Inc.
- Product code
- Code MLD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1025
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beaverton, OR, US
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