DELTEX MEDICAL CARDIOQ EDM— 510(k) K111542
Substantially EquivalentDeltex Medical Limited
FDA 510(k) clearance K111542 for DELTEX MEDICAL CARDIOQ EDM, Substantially Equivalent on 2011-10-20. Applicant: Deltex Medical Limited. Device class: 2.
Clearance details
- Applicant
- Deltex Medical Limited
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hertsfordshire, GB
Recent devices under product code DPW
view allMore clearances from Deltex Medical Limited
view all- K172457 — Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
- K150347 — Deltex Medical CardioQ-EDM, Deltex Medical CardioQ-EDM+
- K142932 — Deltex Medical KDP72 Doppler Probe
- K132139 — DELTEX MEDICAL CARDIOQ-EDM+
- K073593 — I2S DOPPLER PROBE ( 6 HOUR), I2S DOPPLER PROBE (24 HOUR), I2C DOPPLER PROBE (72 HOUR), MODELS 9090-7015, 9090-7016
Data sourced from openFDA. This site is unofficial and independent of the FDA.