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KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012614
510(k) Type
Traditional
Applicant
Medical Instruments Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2002
Days to Decision
261 days
Submission Type
Summary

KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012614
510(k) Type
Traditional
Applicant
Medical Instruments Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2002
Days to Decision
261 days
Submission Type
Summary