Atlas FDA

DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)

FDA 510(k) clearance K071202 · decided 2007-11-30

Clearance details

K-number
K071202
Device name
DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)
Applicant
Dermaport, Inc.
Decision
Unknown
Date received
2007-05-01
Decision date
2007-11-30
Days to decision
213 days
Clearance type
Abbreviated
Product code
MSD
Device class
2
Regulation number
876.5540
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Stoughton, WI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.