NORELCO ANEROID BLOOD PRESSURE METER— 510(k) K811634
Substantially EquivalentNorth American Philips Corp.
FDA 510(k) clearance K811634 for NORELCO ANEROID BLOOD PRESSURE METER, Substantially Equivalent on 1981-06-30. Applicant: North American Philips Corp.. Device class: 2.
Clearance details
- Applicant
- North American Philips Corp.
- 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
- Mchenry, IL, US
Recent devices under product code DXQ
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- 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 North American Philips Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.