The following data is part of a premarket notification filed by Pfizer, Inc. with the FDA for Tape Measure.
| Device ID | K790089 |
| 510k Number | K790089 |
| Device Name: | TAPE MEASURE |
| Classification | Tape, Measuring, Rulers And Calipers |
| Applicant | PFIZER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FTY |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-01-17 |
| Decision Date | 1979-03-06 |