Atlas FDA

CATHETER STRAP

FDA 510(k) clearance K881781 · decided 1988-08-02

Clearance details

K-number
K881781
Device name
CATHETER STRAP
Applicant
Baxter Healthcare Corp
Decision
Substantially Equivalent
Date received
1988-04-26
Decision date
1988-08-02
Days to decision
98 days
Clearance type
Traditional
Product code
KOD
Device class
2
Regulation number
876.5130
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Deerfield Lake, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
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Angled Tip Ureteral Catheter (K181144)Cook Incorporated2018-06-28
Imager II Urology Torque Catheter (K180530)Boston Scientific Corporation2018-04-10
Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter (K171810)Cook Incorporated2018-03-07
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GentleCath Intermittent Urinary Catheter (K172924)Convatec Limited2017-11-21

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Floseal Hemostatic Matrix, Floseal with Recothrom; Floseal Hemostatic Matrix, Floseal Fast Prep; 3 Floseal Hemostatic Ma (P990009/S077)Baxter Healthcare Corp2025-11-13
FLOSEAL MATRIX/FLOSEAL MATRIX HEMOSTATIC SEALANT/PROCEED HEMOSTATIC SEALANT (P990009/S076)Baxter Healthcare Corp2025-06-30
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