Last synced on 23 May 2025 at 11:06 pm

D.C. AMPLIFIER MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770247
510(k) Type
Traditional
Applicant
MENNEN GREATBATCH ELECTONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1977
Days to Decision
7 days

D.C. AMPLIFIER MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770247
510(k) Type
Traditional
Applicant
MENNEN GREATBATCH ELECTONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1977
Days to Decision
7 days