The following data is part of a premarket notification filed by Dana Products, Inc. with the FDA for Dana Reusable Bowie Test Pack For Dana Bowie Dick Indicators.
| Device ID | K120592 |
| 510k Number | K120592 |
| Device Name: | DANA REUSABLE BOWIE TEST PACK FOR DANA BOWIE DICK INDICATORS |
| Classification | Indicator, Physical/chemical Sterilization Process |
| Applicant | DANA PRODUCTS, INC. 7 COREY DR. South Barington, IL 60010 |
| Contact | Harry Bala |
| Correspondent | Harry Bala DANA PRODUCTS, INC. 7 COREY DR. South Barington, 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 | 2012-02-28 |
| Decision Date | 2013-02-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10724995152281 | K120592 | 000 |