CYPRESS MEDICAL PRODUCTS STETHOSCOPE— 510(k) K945082
Substantially EquivalentCypress Medical Products, Ltd.
FDA 510(k) clearance K945082 for CYPRESS MEDICAL PRODUCTS STETHOSCOPE, Substantially Equivalent on 1994-12-08. Applicant: Cypress Medical Products, Ltd.. Device class: 1.
Clearance details
- Applicant
- Cypress Medical Products, Ltd.
- Product code
- Code LDE
- Device class
- Class 1
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mc Henry, IL, US
Recent devices under product code LDE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.