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FDA 510(k), K883346, SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
FDA 510(k), K883346, SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
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510(K) Number: K883346
Device Name: SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
Manufacturer: DIANE RUPPERT
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: 07/28/1988
Date Received: 09/26/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
Manufacturer: DIANE RUPPERT
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: 07/28/1988
Date Received: 09/26/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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