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FCP-11ECG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842169
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
3/13/1984
Days to Decision
0 days

FCP-11ECG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842169
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
3/13/1984
Days to Decision
0 days