VITAL SIGNS MONITOR— 510(k) K101602
Substantially EquivalentCriticare Systems, Inc.
FDA 510(k) clearance K101602 for VITAL SIGNS MONITOR, Substantially Equivalent on 2010-09-01. Applicant: Criticare Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Criticare 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
- Special
- Location
- Waukesha, WI, US
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More clearances from Criticare Systems, Inc.
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