The following data is part of a premarket notification filed by Pacific Dental Corp. with the FDA for Beach Forcep No. 150 And No. 151.
| Device ID | K821781 |
| 510k Number | K821781 |
| Device Name: | BEACH FORCEP NO. 150 AND NO. 151 |
| Classification | Forceps, Tooth Extractor, Surgical |
| Applicant | PACIFIC DENTAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EMG |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-17 |
| Decision Date | 1982-07-02 |