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FDA 510(k), K952682, LOKKI DT
FDA 510(k), K952682, LOKKI DT
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$89.00 USD
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510(K) Number: K952682
Device Name: LOKKI DT
Manufacturer: DIDIER PARZY
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 06/12/1995
Decision Date: 11/14/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: LOKKI DT
Manufacturer: DIDIER PARZY
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 06/12/1995
Decision Date: 11/14/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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