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

ULTRA-BLASTER

K Number: K980726 · Decision May 12, 1998
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
47
Applicant Total
103
Review Days
77

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
ULTRA-BLASTER
K Number
K980726
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6080
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ultradent Products, Inc.
Date Received
February 24, 1998
Decision Date
May 12, 1998
Product Code
KOJ
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
KOJ Airbrush

Similar 510(k) Clearances

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

View all

Other Clearances by Ultradent Products, Inc.

K Number Device Name
K261404 UltraEZ
K240743 Peak Universal Bond
K240694 FORMA Composite (Shade A3D)
K221909 J-Temp
K220471 VALO X, VALO X Accessory Lenses
K211905 UltraCal XS
K211237 UltraTemp Rez II
K210550 VALO Grand Corded and Accessory Lenses
K190627 VALO Grand Corded
K173163 ChlorCid, ChlorCid V, ChlorCid Surf
Search all 103 clearances from Ultradent Products, Inc. →