510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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EATClass II

Tester, Pulp

21 CFR 872.1720 / Dental
FDA source (opens on fda.gov)

EAT is the FDA product code for Tester, Pulp, a class II device type, regulated under 21 CFR 872.1720. As of , FDA records hold 22 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EAT
Device name
Tester, Pulp
Regulation
21 CFR 872.1720
Device class
Class II
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
22
Ingested recalls
0

Clearances, product code EAT

By decision year
22 clearances under product code EAT with a decision year between 1979 and 2002, 1987 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code EAT by decision year
YearClearances
19791
19801
19821
19831
19873
19881
19891
19931
19941
19952
19962
19972
19991
20012
20022

Applicants with the most clearances

Product code EAT
Applicants holding the most 510(k) clearances under product code EAT
ApplicantClearances
Sybron Dental Specialties, Inc.4
Parkell, Inc.3
The Hygenic Company, LLC3
Analytic Technology2
Life-Tech Intl., Inc.2
Heatshield, Inc.1
North Pacific Dental, Inc.1
Specialites Septodont1
Sybron Endo/Analytic1
Tamler-Stoneham Instruments1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 22 companies shown, in name order