The following data is part of a premarket notification filed by Steritec Products, Inc. with the FDA for Instant Readout Chemical Integrator Challenge Pack, Model Lt- 105.
Device ID | K080136 |
510k Number | K080136 |
Device Name: | INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105 |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | STERITEC PRODUCTS, INC. 599 TOPEKA WAY, SUITE 400 Castle Rock, CO 80109 |
Contact | Linda Nelson |
Correspondent | Linda Nelson STERITEC PRODUCTS, INC. 599 TOPEKA WAY, SUITE 400 Castle Rock, CO 80109 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-01-22 |
Decision Date | 2008-08-15 |
Summary: | summary |