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

FORCEP, DISP., A CLAMP

K Number: K771097 · Decision Jul 14, 1977
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
16
Review Days
24

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Basic Information

Device Name
FORCEP, DISP., A CLAMP
K Number
K771097
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 20, 1977
Decision Date
July 14, 1977
Product Code
HTD
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
HTD Forceps

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K831842 DRAVON T CLAMP
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
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