FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

EUREDUC PNEUMATIC DRAINAGE SYSTEM MODEL TP03

K Number: K960902 · Decision Sep 26, 1996
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
2
Review Days
205

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Basic Information

Device Name
EUREDUC PNEUMATIC DRAINAGE SYSTEM MODEL TP03
K Number
K960902
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eureduc
Date Received
March 5, 1996
Decision Date
September 26, 1996
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JOW), ordered by most recent decision date.

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Other Clearances by Eureduc

K Number Device Name
K954788 EUREDUC PNEUMATIC DRAINAGE SYSTEM