BLOOD PRESSURE CUFF— 510(k) K896986
Substantially EquivalentLatex Medical Devices, Inc.
FDA 510(k) clearance K896986 for BLOOD PRESSURE CUFF, Substantially Equivalent on 1990-03-06. Applicant: Latex Medical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Latex Medical Devices, Inc.
- 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
- Brownsville, TX, 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 Latex Medical Devices, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.