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

BEACH ANESTHETIC SYRINGE CARTR. TYPE

K Number: K821782 · Decision Jul 20, 1982
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
44
Applicant Total
22
Review Days
33

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Basic Information

Device Name
BEACH ANESTHETIC SYRINGE CARTR. TYPE
K Number
K821782
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6770
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Pacific Dental Corp.
Date Received
June 17, 1982
Decision Date
July 20, 1982
Product Code
EJI
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
EJI Syringe, Cartridge

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Other Clearances by Pacific Dental Corp.

K Number Device Name
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.
K821785 BEACH AMALGAM CARVER
K821779 BEACH AMALGAM CARRIER, GUN TYPE
K821788 BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHT
K821786 BEACH SCALERS
Search all 22 clearances from Pacific Dental Corp. →