Atlas FDA

Medtronic Model 5492A, 5492V, 5492AL, 5492VL Patient Cables

FDA 510(k) clearance K203556 · decided 2021-07-12

Clearance details

K-number
K203556
Device name
Medtronic Model 5492A, 5492V, 5492AL, 5492VL Patient Cables
Applicant
Medtronic, Inc.
Decision
Substantially Equivalent
Date received
2020-12-07
Decision date
2021-07-12
Days to decision
217 days
Clearance type
Traditional
Product code
DSA
Device class
2
Regulation number
870.2900
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mounds View, MN, 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

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Aurora EV ICD (DVEA3E4) (P220012/S074)Medtronic, Inc.2026-07-31
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