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AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980366
510(k) Type
Traditional
Applicant
AARON MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
29 days
Submission Type
Summary

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980366
510(k) Type
Traditional
Applicant
AARON MEDICAL INDUSTRIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
29 days
Submission Type
Summary