SENSA-CUFF, MODELS INFANT, CHILD, ADULT— 510(k) K022482
Substantially EquivalentGe Medical Systems Information Technologies
FDA 510(k) clearance K022482 for SENSA-CUFF, MODELS INFANT, CHILD, ADULT, Substantially Equivalent on 2002-08-13. Applicant: Ge Medical Systems Information Technologies. Device class: 2.
Clearance details
- Applicant
- Ge Medical Systems Information Technologies
- Product code
- Code DXQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1120
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tampa, FL, US
Recent devices under product code DXQ
view all- K254287 — Medline Reusable Blood Pressure Cuff
- K260747 — YP-710T Series NIBP Cuff; YP-840T Series Disposable Cuff
- K253089 — NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)
- K253964 — Disposable Neonatal NIBP Cuff (U1681S-C51N)
- K251745 — Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)
More clearances from Ge Medical Systems Information Technologies
view allData sourced from openFDA. This site is unofficial and independent of the FDA.