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ENDOCOAGULATOR MODELS 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
K870773
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1987
Days to Decision
134 days

ENDOCOAGULATOR MODELS 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
K870773
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1987
Days to Decision
134 days