Last synced on 16 May 2025 at 11:05 pm

CARDIO-SLIDECOMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790869
510(k) Type
Traditional
Applicant
CREATIVE INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1979
Days to Decision
10 days

CARDIO-SLIDECOMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790869
510(k) Type
Traditional
Applicant
CREATIVE INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1979
Days to Decision
10 days