The following data is part of a premarket notification filed by Mcgaw Laboratories with the FDA for Tape Measure.
| Device ID | K760521 |
| 510k Number | K760521 |
| Device Name: | TAPE MEASURE |
| Classification | Caliper |
| Applicant | MCGAW LABORATORIES 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KTZ |
| CFR Regulation Number | 888.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-26 |
| Decision Date | 1976-11-12 |