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HGM ASPIRATING ENDOOCULAR(TM) PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925663
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1993
Days to Decision
280 days
Submission Type
Statement

HGM ASPIRATING ENDOOCULAR(TM) PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925663
510(k) Type
Traditional
Applicant
HGM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1993
Days to Decision
280 days
Submission Type
Statement