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HR-5000 ELECTROSURGICAL DEVICE FOR NEW INDICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881276
510(k) Type
Traditional
Applicant
IME CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
40 days

HR-5000 ELECTROSURGICAL DEVICE FOR NEW INDICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881276
510(k) Type
Traditional
Applicant
IME CO. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1988
Days to Decision
40 days