Last synced on 25 January 2026 at 3:41 am

MYOMA DRILL 5MM-8383.611

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940844
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1994
Days to Decision
68 days
Submission Type
Statement

MYOMA DRILL 5MM-8383.611

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940844
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1994
Days to Decision
68 days
Submission Type
Statement