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

K30000 DENTAL CHAIR

K Number: K822740 · Decision Sep 28, 1982
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
62
Applicant Total
7
Review Days
19

Basic Information

Device Name
K30000 DENTAL CHAIR
K Number
K822740
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
KAYCOR INTL., LTD.
Date Received
September 9, 1982
Decision Date
September 28, 1982
Product Code
KLC
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
KLC Chair, Dental, With Operative Unit

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KLC), ordered by most recent decision date.

View all

Other Clearances by KAYCOR INTL., LTD.

K Number Device Name
K965072 PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT
K931717 YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY
K832063 ROBIN CORDLESS HANDPIECE
K813348 YOSHIDA RIDO-F, MODEL LM-01
K811210 YOSHIDA-PANOURA 10
K811211 YOSHIDA AP 100