The following data is part of a premarket notification filed by Mcgaw Laboratories with the FDA for Calipers, Mcgaw Skinfold.
| Device ID | K760520 |
| 510k Number | K760520 |
| Device Name: | CALIPERS, MCGAW SKINFOLD |
| Classification | Calibrator, Volume, Gas |
| Applicant | MCGAW LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BXW |
| CFR Regulation Number | 868.1870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-26 |
| Decision Date | 1976-11-12 |