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ProCell Surgical Sponge-Blood Recovery Unit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193361
510(k) Type
Traditional
Applicant
ProCell Surgical, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/1/2020
Days to Decision
180 days
Submission Type
Summary

ProCell Surgical Sponge-Blood Recovery Unit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193361
510(k) Type
Traditional
Applicant
ProCell Surgical, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/1/2020
Days to Decision
180 days
Submission Type
Summary