Last synced on 30 May 2025 at 11:05 pm

RECOMB ECG PREAMPLIFIER/206 069 03

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834600
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1984
Days to Decision
154 days

RECOMB ECG PREAMPLIFIER/206 069 03

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834600
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1984
Days to Decision
154 days