The following data is part of a premarket notification filed by Boehringer Laboratories with the FDA for Boehringer Laboratories Suction Regulator, Modified.
| Device ID | K933232 |
| 510k Number | K933232 |
| Device Name: | BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED |
| Classification | Regulator, Vacuum |
| Applicant | BOEHRINGER LABORATORIES P.O. BOX 870 Norristown, PA 19404 |
| Contact | John Karpowicz |
| Correspondent | John Karpowicz 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 | 1993-07-06 |
| Decision Date | 1994-03-28 |