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

SATELEC PROPHY UNIT PU-2000

K Number: K832673 · Decision Oct 19, 1983
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
11
Review Days
71

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
SATELEC PROPHY UNIT PU-2000
K Number
K832673
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Spelna, Inc.
Date Received
August 9, 1983
Decision Date
October 19, 1983
Product Code
EIA
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
EIA Unit, Operative Dental

Similar 510(k) Clearances

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

View all

Other Clearances by Spelna, Inc.

K Number Device Name
K852525 SATALEC PIEZOTEC
K852527 SATALEC SEPTOSONIC SC 80/SC 120
K852522 SATALEC SERVOTOME
K853200 5X2 SATALEC CHIROPODY CASE
K852524 SATALEC SERVOTORQUE S2 SX2
K852521 SATLEC PROPHY UNIT PU 3055
K832674 SATELEC PROPHY UNIT PU 2000S
K832664 SATELEC SUPRASSON PIEZOMATIC P2
K832665 SATELEC SUPRASSON SP 3055
K820256 MEDILAC #SR4 & SR 40
Search all 11 clearances from Spelna, Inc. →