FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP

K Number: K012650 · Decision Apr 12, 2002
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
341
Applicant Total
14
Review Days
242

Basic Information

Device Name
HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP
K Number
K012650
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HYGIA HEALTH SERVICES, INC.
Date Received
August 13, 2001
Decision Date
April 12, 2002
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOW Sleeve, Limb, Compressible

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Other Clearances by HYGIA HEALTH SERVICES, INC.

K Number Device Name
K100523 ADULT CEREBRAL-SOMATIC OXIMETRY SENSOR, PEDIATRIC CEREBRAL-SOMATIC OXIMETRY SENSOR MODEL HHS-SAFB-SM, HHS-SPFB-USA
K090074 HYGIA HEALTH SERVICES REPROCESSED COMPRESSION SLEEVES / FOOT CUFFS
K080424 HYGIA HEALTH SERVICES REPROCESSED LNCS SENSORS, MODELS HHS-1858, HHS-1862, HHS-1860 AND HHS-1861
K053575 HYGIA HEALTH SERVICES REPROCESSED KENDALL SCD EXPRESS SLEEVES/FOOT CUFFS
K041867 HYGIA HEALTH SERVICES REPROCESSED OXIMAX SENSORS MODEL # HHS-MAX-A, HHS-MAX-AL, HHS-MAX-N
K032821 HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF
K012715 HYGIA HEALTH SERVICES REPROCESSED NELLCOT D-25 OXISENSOR II
K021509 HYGIA HEALTH SERVICES REPROCESSED NOVAMEDIX IMPAB MODELS 5065, 5075, 5087, 5089
K012657 HYGIA HEALTH SERVICES REPROCESSED NUTECH CALF WRAP
K012651 HYGIA HEALTH SERVICES REPROCESSED HUNTLEIGH FOOT WRAP MODELS FG 100, FG 200
Search all 14 clearances from HYGIA HEALTH SERVICES, INC. →