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

DRAVON T CLAMP

K Number: K831842 · Decision Sep 26, 1983
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
16
Review Days
110

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Basic Information

Device Name
DRAVON T CLAMP
K Number
K831842
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dravon Medical, Inc.
Date Received
June 8, 1983
Decision Date
September 26, 1983
Product Code
KDC
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KDC Instrument, Surgical, Disposable

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K812771 PERITONEAL DIALYSIS DRAINAGE
K812772 PERITONEAL DIALYSIS CYCLER SET (8UNIT)
K811851 S-610 SHUNT ADAPTOR SET
K800435 HEMOSTATIC/TUBE OCCLUDING FORCEPS
K782057 CATHETER, RADIOPAQUE TENCKHOFF
K782058 CATHETER, BETA-CAP-PERITONEAL
K781755 DAP-PAK
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