Atlas FDA

PHOENIX DISPOSABLE PRESSURE TRANSDUCER #73-600

FDA 510(k) clearance K925638 · decided 1993-10-18

Clearance details

K-number
K925638
Device name
PHOENIX DISPOSABLE PRESSURE TRANSDUCER #73-600
Applicant
Baxter Healthcare Corp
Decision
Substantially Equivalent
Date received
1992-11-09
Decision date
1993-10-18
Days to decision
343 days
Clearance type
Traditional
Product code
DXO
Device class
2
Regulation number
870.2870
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Santa Ana, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Pressure Monitoring sets with VAMP Plus closed blood sampling system model # T001691A, PXV recall (Z-1146-2013)Edwards Lifesciences, LLC2013-04-18

PMA approvals by this applicant

RecordFirmDate
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Floseal Hemostatic Matrix (P990009/S075)Baxter Healthcare Corp2025-01-30
Adept Adhesion Reduction Solution (P050011/S009)Baxter Healthcare Corp2024-08-23
Floseal Hemostatic Matrix, Floseal with Recothrom, Floseal Hemostatic Matrix, Floseal Fast Prep (P990009/S074)Baxter Healthcare Corp2024-08-15
Floseal Hemostatic Matrix (P990009/S073)Baxter Healthcare Corp2024-01-10
Floseal Hemostatic Matrix, Fast Prep, Floseal Hemostatic Matrix, RTS (P990009/S072)Baxter Healthcare Corp2023-12-12
Floseal Hemostatic Matrix, RT5 (P990009/S070)Baxter Healthcare Corp2023-02-02