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DCG PREAMPLIFIER MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780572
510(k) Type
Traditional
Applicant
C-V MONITORS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1978
Days to Decision
29 days

DCG PREAMPLIFIER MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780572
510(k) Type
Traditional
Applicant
C-V MONITORS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1978
Days to Decision
29 days