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DORNIER LITHOTRIPTER (STATIONARY AND MOBILE)

FDA premarket approval P840008/S064 · decided 1998-06-05

Approval details

PMA number
P840008
Supplement
S064
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
DORNIER LITHOTRIPTER (STATIONARY AND MOBILE)
Generic name
Lithotriptor, extracorporeal shock-wave, urological
Applicant
Dornier Medtech America, Inc.
Date received
1998-05-26
Decision date
1998-06-05
Days to decision
10 days
Decision code
APRL
Product code
LNS
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Kennesaw, GA
Statement
Approval for changes to the therapy head positioning, modifications of the control panel, addition of a servicing modem, changes to the air flow within the device, material changes to the patient table, ECG monitor model replacement, change of the available X-ray features, software modifications, labeling changes, and integration of the water circulation device with its control computer. The device, as modified, will be marketed under the trade name Dorneir Lithotripter S and is indicated for th

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510(k) clearances by this applicant

RecordFirmDate
Delta III Pro (K221903)Dornier Medtech America, Inc.2023-02-22
Dornier Thulio (K213252)Dornier Medtech America, Inc.2022-07-27
Nautilus (K220871)Dornier Medtech America, Inc.2022-04-18
Electrosurgical accessory (K210394)Dornier Medtech America, Inc.2021-05-19
Dornier MAGELLAN Ureteral Access Sheath (K201815)Dornier Medtech America, Inc.2020-11-20
Delta III Lithotripter (K201074)Dornier Medtech America, Inc.2020-09-03
EQUINOX Balloon Dilatation Catheter (K190612)Dornier Medtech America, Inc.2019-12-06
Dornier Ureteral Stent (K190312)Dornier Medtech America, Inc.2019-11-15