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DRYTOUCH SUCTION STIMULATOR PROBE

Page Type
Cleared 510(K)
510(k) Number
K110712
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2011
Days to Decision
106 days
Submission Type
Summary

DRYTOUCH SUCTION STIMULATOR PROBE

Page Type
Cleared 510(K)
510(k) Number
K110712
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2011
Days to Decision
106 days
Submission Type
Summary