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FDA 510(k), K023984, MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIES
FDA 510(k), K023984, MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIES
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510(K) Number: K023984
Device Name: MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIES
Manufacturer: THE OLYMPUS OPTICAL CO.
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 12/02/2002
Decision Date: 01/31/2003
Regulation Medical Specialty: Ear Nose & Throat
Device Name: MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIES
Manufacturer: THE OLYMPUS OPTICAL CO.
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 12/02/2002
Decision Date: 01/31/2003
Regulation Medical Specialty: Ear Nose & Throat
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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