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

STERI-MATE STERILIZABLE HANDPIECE

K Number: K023697 · Decision Nov 6, 2002
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
191
Applicant Total
23
Review Days
2

Basic Information

Device Name
STERI-MATE STERILIZABLE HANDPIECE
K Number
K023697
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4850
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DENTSPLY INTERNATIONAL
Date Received
November 4, 2002
Decision Date
November 6, 2002
Product Code
ELC
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
ELC Scaler, Ultrasonic

Similar 510(k) Clearances

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

View all

Other Clearances by DENTSPLY INTERNATIONAL

K Number Device Name
K122268 ANGLED XIVE MP ABUTMENT, ANGLED ANKYLOS
K061580 ECLIPSE WAX REMOVER
K060837 IN-OVATION C
K053368 INTERPROXIMAL REDUCTION SYSTEM
K052370 CP BRACKET SYSTEM
K052097 CERAM X UNIVERSAL MANO-CERAMIC RESTORATIVE
K050208 FRIADENT ESTHETICAP
K050959 DELTON ILLUMINATING PIT AND FISSURE SEALING
K050386 PRIME & BOND NT DUAL CURE NANO-TECHNOLOGY UNIVERSAL DENTAL ADHESIVE SYSTEM
K041372 SMARTLITE PS PEN-STYLE LED CURING LIGHT
Search all 23 clearances from DENTSPLY INTERNATIONAL →