The following data is part of a premarket notification filed by Boehringer Laboratories with the FDA for Boehringer Lab Suction Interrupter.
| Device ID | K853155 |
| 510k Number | K853155 |
| Device Name: | BOEHRINGER LAB SUCTION INTERRUPTER |
| Classification | Regulator, Vacuum |
| Applicant | BOEHRINGER LABORATORIES P.O. BOX 870 Norristown, PA 19404 |
| Contact | John Boehringer |
| Correspondent | John Boehringer BOEHRINGER LABORATORIES P.O. BOX 870 Norristown, PA 19404 |
| Product Code | KDP |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-29 |
| Decision Date | 1985-10-16 |