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ENDOMED LAPAROSCOPY INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921686
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1994
Days to Decision
721 days
Submission Type
Statement

ENDOMED LAPAROSCOPY INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921686
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1994
Days to Decision
721 days
Submission Type
Statement