Atlas FDA

SURGICAL CLIPPER

FDA 510(k) clearance K910524 · decided 1991-03-28

Clearance details

K-number
K910524
Device name
SURGICAL CLIPPER
Applicant
Baxter Healthcare Corp
Decision
Substantially Equivalent
Date received
1991-02-07
Decision date
1991-03-28
Days to decision
49 days
Clearance type
Traditional
Product code
LWK
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Valencia, CA, 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
3M(TM) SURGICAL SLIPPER, 9660 SERIES (K946162)Wahl Clipper Corp.1995-01-24
SURGICAL PREP RAZOR (K874370)Derma-Safe Co.1987-11-13
SURGICAL PREP RAZOR, STRAIGHT TYPE (K874234)Derma-Safe Co.1987-11-02

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