AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A— 510(k) K003038
Substantially EquivalentAgilent Technologies Deutschland GmbH
FDA 510(k) clearance K003038 for AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A, Substantially Equivalent on 2000-12-15. Applicant: Agilent Technologies Deutschland GmbH. Device class: 2.
Clearance details
- Applicant
- Agilent Technologies Deutschland GmbH
- Product code
- Code OLW
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boeblingen,, DE
Recent devices under product code OLW
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- K001722 — AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD PRESSURE MODULE
- K001333 — AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR, AGILENT NONI
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