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ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871424
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1987
Days to Decision
90 days

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871424
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1987
Days to Decision
90 days