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PROFESS SOFTWARE, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 90 (DEGREES)

FDA 510(k) clearance K141551 · decided 2014-09-08

Clearance details

K-number
K141551
Device name
PROFESS SOFTWARE, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 90 (DEGREES)
Applicant
Stryker Corporate
Decision
Substantially Equivalent
Date received
2014-06-11
Decision date
2014-09-08
Days to decision
89 days
Clearance type
Traditional
Product code
PGW
Device class
2
Regulation number
882.4560
Medical specialty
Neurology
Advisory committee
Neurology
Location
Kalamazoo, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the recall (Z-2071-2017)Stryker Instruments Div. of Stryker Corporation2017-04-19