Atlas FDA

ECONOLITH E3000, MODEL 3000 (SW-6)

FDA 510(k) clearance K040461 · decided 2004-05-25

Clearance details

K-number
K040461
Device name
ECONOLITH E3000, MODEL 3000 (SW-6)
Applicant
Medispec, Ltd.
Decision
Substantially Equivalent
Date received
2004-02-23
Decision date
2004-05-25
Days to decision
92 days
Clearance type
Special
Product code
LNS
Device class
2
Regulation number
876.5990
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Germantown, MD, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ORTHOSPEC EXTRACORPOREAL SHOCK WAVE THERAPY DEVICE (P040026)Medispec, Ltd.2005-04-01
ECONOLITH LITHOTRIPTER (P950043/S006)Medispec, Ltd.1999-08-27
ECONOLITH(TM) LITHOTRIPTER (P950043/S005)Medispec, Ltd.1998-09-14
ECONOLITH(TM) LITHOTRIPTER (P950043/S004)Medispec, Ltd.1998-05-21
ECONOLITH(TM) LITHOTRIPTER (P950043/S002)Medispec, Ltd.1998-05-05
ECONOLITH(TM) LITHOTRIPTER (P950043/S001)Medispec, Ltd.1997-06-30
ECONOLITH(TM) LITHOTRIPTER (P950043)Medispec, Ltd.1997-04-07