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

VED VALU- VACUUM ERECTION DEVICE

K Number: K980948 · Decision Jun 25, 1998
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
86
Applicant Total
1
Review Days
104

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Basic Information

Device Name
VED VALU- VACUUM ERECTION DEVICE
K Number
K980948
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5020
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mission Pharmacal Comp
Date Received
March 13, 1998
Decision Date
June 25, 1998
Product Code
LKY
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
LKY Device, External Penile Rigidity

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