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MULTICLIP DISP. LIGATING CLIP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820999
510(k) Type
Traditional
Applicant
DAVIS & GECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1982
Days to Decision
35 days

MULTICLIP DISP. LIGATING CLIP DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820999
510(k) Type
Traditional
Applicant
DAVIS & GECK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1982
Days to Decision
35 days