SURESIGNS VS3, SURESIGNS VS4— 510(k) K133961
Substantially EquivalentPhilips Medical Systems
FDA 510(k) clearance K133961 for SURESIGNS VS3, SURESIGNS VS4, Substantially Equivalent on 2014-06-26. Applicant: Philips Medical Systems. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems
- Product code
- Code DSJ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.