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

FD5000 DENTAL CHAIR

K Number: K896602 · Decision Feb 14, 1990
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
7
Review Days
85

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FD5000 DENTAL CHAIR
K Number
K896602
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Oriola OY Finndent
Date Received
November 21, 1989
Decision Date
February 14, 1990
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 Oriola OY Finndent

K Number Device Name
K893890 FD4500 (DENTAL CHAIR)
K893944 FD 300 DENTAL STOOL
K893943 FD 200 DENTAL STOOL
K893889 FD3500 (DENTAL CHAIR)
K893945 FD 350 DENTAL STOOL
K893946 FD 400 DENTAL STOOL