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

FEATHER-LITE URINARY DIV. POUCH

K Number: K792139 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
101
Applicant Total
373
Review Days
22

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Basic Information

Device Name
FEATHER-LITE URINARY DIV. POUCH
K Number
K792139
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
October 22, 1979
Decision Date
November 13, 1979
Product Code
EXB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EXB Collector, Ostomy

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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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