KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN— 510(k) K012614
Substantially EquivalentMedical Instruments Technology, Inc.
FDA 510(k) clearance K012614 for KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN, Substantially Equivalent on 2002-05-01. Applicant: Medical Instruments Technology, Inc..
Clearance details
- Applicant
- Medical Instruments Technology, Inc.
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. George, UT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.