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

DEKNATEL DISPOSABLE GOOSEN VASCULAR PNCH

K Number: K820258 · Decision Mar 2, 1982
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
373
Review Days
29

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Basic Information

Device Name
DEKNATEL DISPOSABLE GOOSEN VASCULAR PNCH
K Number
K820258
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
February 1, 1982
Decision Date
March 2, 1982
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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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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