The following data is part of a premarket notification filed by Dana Products, Inc. with the FDA for Dana Reusable Test Pack For Steam Sterilization.
Device ID | K102761 |
510k Number | K102761 |
Device Name: | DANA REUSABLE TEST PACK FOR STEAM STERILIZATION |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | DANA PRODUCTS, INC. 7 COREY DR. South Barrington, IL 60010 |
Contact | Harry Bala |
Correspondent | Harry Bala DANA PRODUCTS, INC. 7 COREY DR. South Barrington, IL 60010 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-23 |
Decision Date | 2010-12-20 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00724995152246 | K102761 | 000 |
00724995152239 | K102761 | 000 |