CAPILLARY PERFUSION MONITOR #LD5000— 510(k) K812005
Substantially EquivalentNuclear Pacific, Inc.
FDA 510(k) clearance K812005 for CAPILLARY PERFUSION MONITOR #LD5000, Substantially Equivalent on 1982-02-04. Applicant: Nuclear Pacific, Inc.. Device class: 2.
Clearance details
- Applicant
- Nuclear Pacific, Inc.
- 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
- Mchenry, IL, US
Recent devices under product code DPW
view allData sourced from openFDA. This site is unofficial and independent of the FDA.