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

GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX

K Number: K863009 · Decision Sep 25, 1986
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
10
Applicant Total
21
Review Days
48

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
GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX
K Number
K863009
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3150
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sds Dental, Inc.
Date Received
August 8, 1986
Decision Date
September 25, 1986
Product Code
EJP
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
EJP Articulators

Similar 510(k) Clearances

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

View all

Other Clearances by Sds Dental, Inc.

K Number Device Name
K990546 DELSONIC 2000
K990545 JETSONIC 2000
K964619 DELIVERY SYSTEM(SDS 1400 XL)/DELIVERY SYSTEM CUSPIDOR(SDS1450,SDS1650 XL)
K902864 SURGICAL LIGHTING-CENTRA 450
K902865 BAUMER SURGICAL TABLE
K863011 DENTATUS LS/EUROFLEX F-IV/ISOLIGHT REFLECT/CM-II
K863021 CM-II, CM-I WATER UNIT
K863016 DENTATUS L SET
K863007 EUROFLEX F-IV, ISOFLEX III
K863015 ISOPRAT C-III SET/ISOCART III AUXILIARY UNIT
Search all 21 clearances from Sds Dental, Inc. →