Last synced on 20 January 2023 at 11:05 pm

REMUSK MP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922029
510(k) Type
Traditional
Applicant
EQUIPEMENT BIOMEDICAL SPECIALISE, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/6/1992
Days to Decision
158 days
Submission Type
Summary

REMUSK MP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922029
510(k) Type
Traditional
Applicant
EQUIPEMENT BIOMEDICAL SPECIALISE, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/6/1992
Days to Decision
158 days
Submission Type
Summary