Atlas FDA

RF TUNNELER WIRE

FDA 510(k) clearance K051670 · decided 2006-03-30

Clearance details

K-number
K051670
Device name
RF TUNNELER WIRE
Applicant
Baylis Medical Co., Inc.
Decision
Substantially Equivalent
Date received
2005-06-22
Decision date
2006-03-30
Days to decision
281 days
Clearance type
Traditional
Product code
PDU
Device class
2
Regulation number
870.1250
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mississauga, Ontario, CA
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.