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exCellerator Cervical Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182049
510(k) Type
Traditional
Applicant
ExCell Company LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
268 days
Submission Type
Summary

exCellerator Cervical Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182049
510(k) Type
Traditional
Applicant
ExCell Company LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
268 days
Submission Type
Summary