The following data is part of a premarket notification filed by Cardinal Scale Mfg. Co. with the FDA for Detecto Model 6700 Series.
| Device ID | K924847 |
| 510k Number | K924847 |
| Device Name: | DETECTO MODEL 6700 SERIES |
| Classification | Scale, Patient |
| Applicant | CARDINAL SCALE MFG. CO. P.O. BOX 151 203 EAST DAUGBERTY Webb City, MO 64870 |
| Contact | Terry James |
| Correspondent | Terry James CARDINAL SCALE MFG. CO. P.O. BOX 151 203 EAST DAUGBERTY Webb City, MO 64870 |
| Product Code | FRW |
| CFR Regulation Number | 880.2720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-28 |
| Decision Date | 1993-05-24 |