Last synced on 24 June 2022 at 11:05 pm

MODEL 508 PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921309
510(k) Type
Traditional
Applicant
CRITICARE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1993
Days to Decision
647 days
Submission Type
Statement

MODEL 508 PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921309
510(k) Type
Traditional
Applicant
CRITICARE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1993
Days to Decision
647 days
Submission Type
Statement