Last synced on 20 December 2024 at 11:05 pm

SILIMED NASAL RETAINER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980221
510(k) Type
Traditional
Applicant
SILIMED, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1998
Days to Decision
70 days
Submission Type
Summary

SILIMED NASAL RETAINER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980221
510(k) Type
Traditional
Applicant
SILIMED, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1998
Days to Decision
70 days
Submission Type
Summary