Atlas FDA

ROCAMED ROCAUS PLATINUM

FDA 510(k) clearance K120160 · decided 2012-05-14

Clearance details

K-number
K120160
Device name
ROCAMED ROCAUS PLATINUM
Applicant
Promepla Sam
Decision
Substantially Equivalent
Date received
2012-01-19
Decision date
2012-05-14
Days to decision
116 days
Clearance type
Traditional
Product code
KNY
Device class
2
Regulation number
876.5130
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Monaco, MC
Third-party review
No
Expedited review
No

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VARI-PASS VARIABLE LENGTH ACCESS SHEATH (K123170)Olympus Surgical Technologies America2013-02-04
PREFILLED CATHETER INFLATION SYRINGE (K112209)Avail Medical Products, Inc.2011-09-08
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CYSTOGLIDE INTRODUCER SHEATH (K052298)Percutaneous Systems, Incorporated2006-12-12
CAREVENT (K062240)Chief Medical, LLC2006-10-16

Recalls involving this device

No recalls on record reference this clearance.