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

BA-93

K Number: K811407 · Decision Jun 16, 1981
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
46
Review Days
28

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
BA-93
K Number
K811407
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Deringer-Ney, Inc.
Date Received
May 19, 1981
Decision Date
June 16, 1981
Product Code
EJH
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
EJH Alloy, Metal, Base

Similar 510(k) Clearances

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

View all

Other Clearances by Deringer-Ney, Inc.

K Number Device Name
K933178 GDC 3509
K930482 DENTAL CASTING ALLOY, MODIFICATION - PF-3
K930481 DENTAL CASTING ALLOY MODIFICATION-PF-4
K925273 GDC 3445
K920922 GDC 3367
K920060 DENTAL SOLDER ALLOY
K920887 GDC-3338, DENTAL SOLDER ALLOY
K910065 GDC-3200 DENTAL SOLDER
K904695 GDC-1501
K904614 GDC-1475
Search all 46 clearances from Deringer-Ney, Inc. →