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

VET-CO OTC VACUUM DEVICE/VET-CO CONSTRICTION RING SET

K Number: K974215 · Decision Feb 19, 1998
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
86
Applicant Total
2
Review Days
101

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VET-CO OTC VACUUM DEVICE/VET-CO CONSTRICTION RING SET
K Number
K974215
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5020
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vetco, Inc.
Date Received
November 10, 1997
Decision Date
February 19, 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

Similar 510(k) Clearances

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

View all

Other Clearances by Vetco, Inc.

K Number Device Name
K902240 VET (VACUUM ERECTION TECHNOLOGY)