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

BEACH CURETTE NO. 2 AND NO. 3 T.G.

K Number: K821789 · Decision Jul 6, 1982
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
6
Applicant Total
22
Review Days
19

Basic Information

Device Name
BEACH CURETTE NO. 2 AND NO. 3 T.G.
K Number
K821789
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
PACIFIC DENTAL CORP.
Date Received
June 17, 1982
Decision Date
July 6, 1982
Product Code
EMS
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
EMS Curette, Periodontic

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K Number Device Name
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K821786 BEACH SCALERS
K821783 BEACH SILICATE FILLING & LINING APPLIC.
K821784 BEACH GINGIVAL RETRACTION INSTR. TYPE B
K821777 BEACH MOUTH MIRROR
K821780 BEACH EXPLORER NO. 23T.G.
K821788 BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHT
K821779 BEACH AMALGAM CARRIER, GUN TYPE
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