Last synced on 23 September 2022 at 11:05 pm

NGM FRAME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911644
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
324 days

NGM FRAME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911644
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
324 days