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ESWALLOW DYSPHAGIA THERAPY KIT, PMI DYSPHAGIA THERAPY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092202
510(k) Type
Traditional
Applicant
ESWALLOW USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
568 days
Submission Type
Summary

ESWALLOW DYSPHAGIA THERAPY KIT, PMI DYSPHAGIA THERAPY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092202
510(k) Type
Traditional
Applicant
ESWALLOW USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
568 days
Submission Type
Summary