Last synced on 20 December 2024 at 11:05 pm

ACU-PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842946
510(k) Type
Traditional
Applicant
ACUTEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1984
Days to Decision
134 days

ACU-PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842946
510(k) Type
Traditional
Applicant
ACUTEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1984
Days to Decision
134 days