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ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852683
510(k) Type
Traditional
Applicant
AMERICAN BENTLEY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1985
Days to Decision
48 days

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852683
510(k) Type
Traditional
Applicant
AMERICAN BENTLEY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1985
Days to Decision
48 days