Last synced on 16 May 2025 at 11:05 pm

DYONICS DRILL GUIDE/ISOMETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880739
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1988
Days to Decision
26 days

DYONICS DRILL GUIDE/ISOMETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880739
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1988
Days to Decision
26 days