FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MONOJECT PULP-CAPPING MATERIAL

K Number: K791088 · Decision Oct 22, 1979
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
76
Applicant Total
191
Review Days
132

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Basic Information

Device Name
MONOJECT PULP-CAPPING MATERIAL
K Number
K791088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sherwood Medical Co.
Date Received
June 12, 1979
Decision Date
October 22, 1979
Product Code
EJK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EJK Liner, Cavity, Calcium Hydroxide

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K955831 ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM
K954429 KANGAROO ENTRISTAR SKIN-LEVEL GASTROSTOMY KIT
K954525 SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
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Search all 191 clearances from Sherwood Medical Co. →