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DRYTOUCH SUCTION STIMULATOR PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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