Last synced on 11 July 2025 at 11:06 pm

PRESS-MATE PM-2100 VITAL SIGN MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022537
510(k) Type
Traditional
Applicant
COLIN MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2002
Days to Decision
43 days
Submission Type
Summary

PRESS-MATE PM-2100 VITAL SIGN MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022537
510(k) Type
Traditional
Applicant
COLIN MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2002
Days to Decision
43 days
Submission Type
Summary