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

BEACH AMALGAM CARVER

K Number: K821785 · Decision Jul 6, 1982
Classifications
1
FEI Numbers
91
Registration Numbers
91
Same Product Code
2
Applicant Total
22
Review Days
19

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Basic Information

Device Name
BEACH AMALGAM CARVER
K Number
K821785
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
EKH
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
EKH Carver, Dental Amalgam, Operative

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Other Clearances by Pacific Dental Corp.

K Number Device Name
K821782 BEACH ANESTHETIC SYRINGE CARTR. TYPE
K821783 BEACH SILICATE FILLING & LINING APPLIC.
K821790 BEACH EXCAVATOR'S NO. 1 & NO. 2
K821789 BEACH CURETTE NO. 2 AND NO. 3 T.G.
K821784 BEACH GINGIVAL RETRACTION INSTR. TYPE B
K821777 BEACH MOUTH MIRROR
K821780 BEACH EXPLORER NO. 23T.G.
K821779 BEACH AMALGAM CARRIER, GUN TYPE
K821788 BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHT
K821786 BEACH SCALERS
Search all 22 clearances from Pacific Dental Corp. →