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subpart-b—diagnostic-devices/

RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K885211
510(k) Type: Traditional
Applicant: RF DESIGN ASSOC., INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 6/13/1989
Days to Decision: 181 days

FDA Browser

subpart-b—diagnostic-devices/

RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K885211
510(k) Type: Traditional
Applicant: RF DESIGN ASSOC., INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 6/13/1989
Days to Decision: 181 days