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DAVOL LAPAROSCOPIC INSUFFLATION NEEDLE FOR GENERAL LAPAROSCOPIC PROCEDURES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936102
510(k) Type
Traditional
Applicant
DAVOL, INC., SUB. C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1994
Days to Decision
146 days
Submission Type
Summary