Atlas FDA

UROSURGE PERCUTANEOUS SANS (STOLLER AFFERENT NERVE STIMULATOR) DEVICE

FDA 510(k) clearance DEN000002 · decided 2000-02-09

Clearance details

K-number
DEN000002
Device name
UROSURGE PERCUTANEOUS SANS (STOLLER AFFERENT NERVE STIMULATOR) DEVICE
Applicant
Urosurge, Inc.
Decision
Unknown
Date received
2000-01-27
Decision date
2000-02-09
Days to decision
13 days
Clearance type
Post-NSE
Product code
NAM
Device class
2
Regulation number
876.5310
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Coralville, IA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.