FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PRESSURIZER, EXETER CEMENT

K Number: K781792 · Decision Feb 8, 1979
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
7
Applicant Total
373
Review Days
106

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Basic Information

Device Name
PRESSURIZER, EXETER CEMENT
K Number
K781792
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2240
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
October 25, 1978
Decision Date
February 8, 1979
Product Code
KIZ
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KIZ Dish, Tissue Culture

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Other Clearances by Howmedica Corp.

K Number Device Name
K983528 MICRO DYNAMIC MESH
K983404 TYPE 3 FEMORAL COMPONENTS
K980925 DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
K980926 DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION
K980632 DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION
K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
K983419 HOFFMANN II MIAMI POST
K982958 ZETA MULTIZONE LOCKING NAIL SYSTEM
K982873 ZETA MULTIZONE SCN LOCKING NAIL
K982531 HOWMEDICA LEIBINGER RESORBABLE FIXATION SYSTEM
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