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MYOMA DRILL 5MM-8383.611

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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