The following data is part of a premarket notification filed by Analytic Technology with the FDA for Pulptester Model 2001.
Device ID | K790799 |
510k Number | K790799 |
Device Name: | PULPTESTER MODEL 2001 |
Classification | Tester, Pulp |
Applicant | ANALYTIC TECHNOLOGY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EAT |
CFR Regulation Number | 872.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-04-24 |
Decision Date | 1979-05-31 |