Last synced on 2 December 2022 at 11:04 pm

DUAL-AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860949
510(k) Type
Traditional
Applicant
VITALOGRAPH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1986
Days to Decision
55 days

DUAL-AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860949
510(k) Type
Traditional
Applicant
VITALOGRAPH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1986
Days to Decision
55 days