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

SURGICAL CURETTE, VARIOUS

K Number: K841004 · Decision May 11, 1984
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
10
Applicant Total
41
Review Days
63

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Basic Information

Device Name
SURGICAL CURETTE, VARIOUS
K Number
K841004
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Premier Dental Products Co.
Date Received
March 9, 1984
Decision Date
May 11, 1984
Product Code
HCY
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HCY Curette, Uterine

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K062683 ENAMEL PRO VARNISH
K062166 ENAMEL PRO
K061997 PREMIER SELF-ETCHING ENAMEL SEALANT
K061998 PREMIER SELF-ETCHING BOND ENHANCER
K051866 PREMIER TEMPORARY CEMENT
K042215 RADIOPAQUE, GLASS IONOMER ENDODONTIC CEMENT
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