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EDENTEC MODEL 2000W OPTION S CARDIO-RESP. PROCESS.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884614
510(k) Type
Traditional
Applicant
EDENTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1989
Days to Decision
89 days

EDENTEC MODEL 2000W OPTION S CARDIO-RESP. PROCESS.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884614
510(k) Type
Traditional
Applicant
EDENTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1989
Days to Decision
89 days