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

PALL DENTAL FILTRATION SYSTEM WITH INLINE HANDPIECE HOUSING AND FILTER MEMBRANE

K Number: K983731 · Decision Dec 21, 1998
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
6
Review Days
60

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
PALL DENTAL FILTRATION SYSTEM WITH INLINE HANDPIECE HOUSING AND FILTER MEMBRANE
K Number
K983731
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pall Medical
Date Received
October 22, 1998
Decision Date
December 21, 1998
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 Pall Medical

K Number Device Name
K033991 MODIFICATION TO LAPAROSHIELD CONDITIONED INSUFFLATION SET
K030469 LAPAROSHIELD CONDITIONED INSUFFLATION SET
K013093 PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
K992361 PALL SURGICLEAR LAPAROSCOPIC SMOKE FILTRATION SYSTEM, MODEL CLSF1
K983735 PALL DENTAL FILTRATION SYSTEM WITH AIR WATER SYRINGE HOUSING AND FILTER MEMBRANE