The following data is part of a premarket notification filed by Carr Metal Products, Inc. with the FDA for Carr Rigid Container System.
| Device ID | K972138 |
| 510k Number | K972138 |
| Device Name: | CARR RIGID CONTAINER SYSTEM |
| Classification | Wrap, Sterilization |
| Applicant | CARR METAL PRODUCTS, INC. 3735 NORTH ARLINGTON AVE. Indianapolis, IN 46218 |
| Contact | Alan Booker |
| Correspondent | Alan Booker CARR METAL PRODUCTS, INC. 3735 NORTH ARLINGTON AVE. Indianapolis, IN 46218 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-06 |
| Decision Date | 1997-11-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| D6919010924 | K972138 | 000 |
| D6919010908 | K972138 | 000 |
| D6919010904 | K972138 | 000 |
| D6919010901 | K972138 | 000 |
| 00348783011500 | K972138 | 000 |
| 00348783011494 | K972138 | 000 |
| 00348783011487 | K972138 | 000 |
| 00348783011470 | K972138 | 000 |