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FORCEPS, BIOPSY, GASTROINTESTINAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934186
510(k) Type
Traditional
Applicant
PRIMED INSTRUMENTS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/14/1993
Days to Decision
110 days
Submission Type
Statement

FORCEPS, BIOPSY, GASTROINTESTINAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934186
510(k) Type
Traditional
Applicant
PRIMED INSTRUMENTS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/14/1993
Days to Decision
110 days
Submission Type
Statement