The following data is part of a premarket notification filed by Hill Engineering with the FDA for Pm-pager.
| Device ID | K933552 |
| 510k Number | K933552 |
| Device Name: | PM-PAGER |
| Classification | Monitor, Bed Patient |
| Applicant | HILL ENGINEERING 41 HIGH RIDGE RD. Boxford, MA 01921 |
| Contact | Joseph C Hill |
| Correspondent | Joseph C Hill HILL ENGINEERING 41 HIGH RIDGE RD. Boxford, MA 01921 |
| Product Code | KMI |
| CFR Regulation Number | 880.2400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-21 |
| Decision Date | 1994-09-22 |